Data / Medical devices / United States / Nasorcap Medical, Inc.
Nasorcap Medical, Inc.: FDA-registered device maker in Venetia, PA, United States, 1 510(k) clearance
Nasorcap Medical, Inc. is registered with the FDA (registration 2529489) in Venetia, PA, United States. It lists 4 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 14, 1992. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2529489
- FEI number
- 1000121431
- Address
- 105 Harvest Circle, Venetia, PA, United States, 15367
- Owner or operator
- NASORCAP MEDICAL, INC. (9003303)
- Roles
- Manufacturer
- First device listed
- October 5, 2007
- Registered through
- 2026
- Brand names listed
- AirWave, Bite Guard, NAZORCAP Bite Guard, NAZORCAP Sampler
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Airway, Oropharyngeal, Anesthesiology | CAE | 1 | Manufacturer | accessdata.fda.gov |
| Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase | CCK | 2 | Manufacturer | accessdata.fda.gov |
| Endoscopic Bite Block | MNK | 1 | Manufacturer | accessdata.fda.gov |
| Protector, Dental | BRW | 1 | 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 14, 1992 | K911970 | NASAL/ORAL 02 DELIVERY AND GAS SAMPLING DEVICE | CCK | Substantially Equivalent | Nasorcap Ent., Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Endoscopic Bite Block
- All makers of Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
- All makers of Protector, Dental
- All makers of Airway, Oropharyngeal, Anesthesiology
Updated August 14, 1992. 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.