Data / Medical devices / United States / Responsive Respiratory Inc.
Responsive Respiratory Inc.: FDA-registered device maker in Saint Louis, MO, United States, 5 510(k) clearances
Responsive Respiratory Inc. is registered with the FDA (registration 3005380088) in Saint Louis, MO, United States. It lists 9 device types. The FDA files 5 510(k) clearances under its listings, the newest dated July 24, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3005380088
- Address
- 6244 Lemay Ferry Rd, Saint Louis, MO, United States, 63129
- Owner or operator
- RESPONSIVE RESPIRATORY INC. (9089133)
- Roles
- Complaint file establishment, Remanufacturer, Repackager or relabeler, Specification developer
- First device listed
- September 5, 2006
- Registered through
- 2026
- Brand names listed
- CYL-FIL OXYGEN SYSTEM, Cylinder, compressed gas, and valve, Oxygen Conserving Device, Oxygen Tubing - Responsive Respiratory, Purify O3, Respond C5 Conserver, Responsive Respiratory Carry Case, Responsive Respiratory Flowmeter and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cannula, Nasal, Oxygen | CAT | 1 | Repackager or relabeler | accessdata.fda.gov |
| Cart, Emergency, Cardiopulmonary (Excluding Equipment) | BZN | 1 | Repackager or relabeler | accessdata.fda.gov |
| Conserver, Oxygen | NFB | 2 | Complaint file establishment, Remanufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Cylinder, Compressed Gas, And Valve | ECX | 1 | Repackager or relabeler | accessdata.fda.gov |
| Disinfectant, Medical Devices | LRJ | 1 | Repackager or relabeler | accessdata.fda.gov |
| Flowmeter, Tube, Thorpe, Back-Pressure Compensated | CAX | 1 | Repackager or relabeler | accessdata.fda.gov |
| Oximeter | DQA | 2 | Repackager or relabeler | accessdata.fda.gov |
| Regulator, Pressure, Gas Cylinder | CAN | 1 | Repackager or relabeler | accessdata.fda.gov |
| Stand, Infusion | FOX | 1 | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| July 24, 2025 | K250322 | Respond OC Conserving Regulator (130-0800) | NFB | Substantially Equivalent | Responsive Respiratory | accessdata.fda.gov |
| January 14, 2008 | K072825 | FINGERTIP PULSE OXIMETER, MODEL MD300I | DQA | Substantially Equivalent | Beijing Choice Electronic Technololgy Co., Ltd. | accessdata.fda.gov |
| May 7, 2007 | K070740 | CHAD THERAPEUTICS BONSAI MODEL 800 | NFB | Substantially Equivalent | Chad Therapeutics, Inc. | accessdata.fda.gov |
| September 7, 2006 | K061785 | CYL-FIL OXYGEN SYSTEM | CAN | Substantially Equivalent | Responsive Respiratory, Inc. | accessdata.fda.gov |
| July 18, 2006 | K060751 | INOVO, INC. ACCUPULSE SINGLE LUMEN CONSERVING REGULATOR | NFB | Substantially Equivalent | Inovo, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Regulator, Pressure, Gas Cylinder
- All makers of Conserver, Oxygen
- All makers of Oximeter
- All makers of Flowmeter, Tube, Thorpe, Back-Pressure Compensated
- All makers of Cannula, Nasal, Oxygen
- All makers of Stand, Infusion
Updated July 24, 2025. 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.