Data / Medical devices / United States / Anesthesia Associates, Inc.
Anesthesia Associates, Inc.: FDA-registered device maker in San Marcos, CA, United States, 9 510(k) clearances
Anesthesia Associates, Inc. is registered with the FDA (registration 2022648) in San Marcos, CA, United States. It lists 31 device types. The FDA files 9 510(k) clearances under its listings, the newest dated August 13, 2007. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 2022648
- Address
- 460 Enterprise Street, San Marcos, CA, United States, 92078
- Owner or operator
- Anesthesia Associates, Inc (2022648)
- Roles
- Contract manufacturer, Manufacturer, Remanufacturer, Repackager or relabeler, Specification developer
- First device listed
- December 9, 1992
- Registered through
- 2026
- Brand names listed
- AA Non-Rebreathing Valve 90-Deg, AMBU Type, Accessory, Adapter, Adapters, Aillon Forceps - Aillon Tube Bender, AincA, AincA VideoStylet and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Absorber, Carbon-Dioxide | BSF | 1 | Manufacturer | accessdata.fda.gov |
| Airway, Oropharyngeal, Anesthesiology | CAE | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Apparatus, Gas-Scavenging | CBN | 2 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Attachment, Breathing, Positive End Expiratory Pressure | BYE | 2 | Contract manufacturer, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Bag, Reservoir | BTC | 1 | Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Blood Pressure Cuff | DXQ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Brush, Cleaning, Tracheal Tube | EPE | 1 | Repackager or relabeler | accessdata.fda.gov |
| Circuit, Breathing (W Connector, Adaptor, Y Piece) | CAI | 1 | Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Circulator, Breathing-Circuit | CAG | 2 | Manufacturer | accessdata.fda.gov |
| Connector, Airway (Extension) | BZA | 1 | Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Cuff, Tracheal Tube, Inflatable | BSK | 2 | Repackager or relabeler | accessdata.fda.gov |
| Forceps, Tube Introduction | BWB | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Laryngoscope, Non-Rigid | CAL | 1 | Repackager or relabeler | accessdata.fda.gov |
| Laryngoscope, Rigid | CCW | 1 | Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Mask, Gas, Anesthetic | BSJ | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Meter, Peak Flow, Spirometry | BZH | 2 | Repackager or relabeler | accessdata.fda.gov |
| Monitor, Airway Pressure (Includes Gauge And/Or Alarm) | CAP | 2 | Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Nebulizer, Medicinal, Non-Ventilatory (Atomizer) | CCQ | 1 | Manufacturer | accessdata.fda.gov |
| Oximeter | DQA | 2 | Repackager or relabeler | accessdata.fda.gov |
| Protector, Dental | BRW | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Spirometer, Diagnostic | BZG | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Spirometer, Monitoring (W/Wo Alarm) | BZK | 2 | Manufacturer, Remanufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Stethoscope Head | BZS | 1 | Contract manufacturer, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Stimulator, Nerve, Battery-Powered | BXN | 2 | Contract manufacturer, Manufacturer, Specification developer | accessdata.fda.gov |
| Stylet, Tracheal Tube | BSR | 1 | Contract manufacturer, Manufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Support, Breathing Tube | JAY | 1 | Contract manufacturer, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Valve, Non-Rebreathing | CBP | 2 | Contract manufacturer, Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Valve, Switching (Ploss) | JFE | 1 | Contract manufacturer, Manufacturer | accessdata.fda.gov |
| Vaporizer, Anesthesia, Non-Heated | CAD | 2 | Manufacturer | accessdata.fda.gov |
| Ventilator, Emergency, Manual (Resuscitator) | BTM | 2 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Ventilator, Emergency, Powered (Resuscitator) | BTL | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 13, 2007 | K070371 | FINGERTIP PULSE OXIMETER MD300C | DQA | Substantially Equivalent | Beijing Choice Electronic Technololgy Co., Ltd. | accessdata.fda.gov |
| December 23, 2005 | K053140 | AMBU MARK IV RESUSCITATOR | BTM | Substantially Equivalent | Ambu A/S | accessdata.fda.gov |
| December 29, 1995 | K954438 | SUNMED'S GREENLINE FIBER OPTIC LARYNGOSCOPE | CCW | Substantially Equivalent | Rms Div. | accessdata.fda.gov |
| October 13, 1992 | K921926 | JET VENTILATOR/JETTING DEVICE | BTL | Substantially Equivalent | Anesthesia Assoc., Inc. | accessdata.fda.gov |
| July 20, 1991 | K912723 | POSEY CUFFLATOR | BSK | Substantially Equivalent | Posey Co. | accessdata.fda.gov |
| January 4, 1991 | K903674 | MODEL 295 ELECTRONIC RESPIROMETER | BZK | Substantially Equivalent | National Medical Sales, Inc. | accessdata.fda.gov |
| October 29, 1985 | K851265 | PEAK FLOWMETERS FOR SPIROMETRY | BZH | Substantially Equivalent | Solcoor, Inc. | accessdata.fda.gov |
| December 27, 1983 | K833871 | UNIVERSAL CONTROL ARM | CAI | Substantially Equivalent | Anesthesia Assoc., Inc. | accessdata.fda.gov |
| June 18, 1981 | K811614 | NERVE STIMULATOR MODEL AA 1050 | BXN | Substantially Equivalent | Anesthesia Assoc., Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Attachment, Breathing, Positive End Expiratory Pressure
- All makers of Valve, Non-Rebreathing
- All makers of Laryngoscope, Non-Rigid
- All makers of Stimulator, Nerve, Battery-Powered
- All makers of Apparatus, Gas-Scavenging
- All makers of Circuit, Breathing (W Connector, Adaptor, Y Piece)
Updated August 13, 2007. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.