Vmax 29122-507
Vmax 29122-507 is a pulmonary function analysis system (FDA Class II; FDA product code BTY, Calculator, Predicted Values, Pulmonary Function) made by Vyaire Medical, Inc., cleared under FDA 510(k) K942211 on 22 Nov 1994 and listed in FDA GUDID since 20 Jul 2021 (UDI-DI 10190752168244), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10190752168244 | Date20 Jul 2021 | StatusListed |
| United States | FDA 510(k)SESE | NumberK942211 | Date22 Nov 1994 | StatusActive |
Official records
- AccessGUDID record 10190752168244
- FDA 510(k) database K942211
Across registries
- FDA 510(k) K942211 decided 22 Nov 1994 Active
- FDA GUDID UDI-DI 10190752168244 listed 20 Jul 2021 Listed
Timeline
- Cleared FDA 510(k) K942211
- Listed FDA GUDID 10190752168244
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Vmax
- Generic name
- Pulmonary function analysis system, adult
- Model / Ref / Catalog
- 29122-507
- Primary DI / UDI-DI
- 10190752168244
- 510(k) Number
- FDA product code
- BTY
- GMDN term
- Pulmonary function analysis system, adult
- Device class
- Class II
- Regulation number
- 868.1890
- GUDID distribution status
- In Commercial Distribution
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