Vyaire 707230
by Jaeger Medical GmbH 2 variants
Vyaire 707230 is a Class II device made by Jaeger Medical GmbH, cleared under FDA 510(k) K072323 on 10 Oct 2007 and listed in FDA GUDID since 19 Mar 2019 (UDI-DI 14250892903986), 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 | Number14250892903986 | Date19 Mar 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK072323 | Date10 Oct 2007 | StatusActive |
Official records
- AccessGUDID record 14250892903986
- FDA 510(k) database K072323
Across registries
- FDA 510(k) K072323 decided 10 Oct 2007 Active
- FDA GUDID UDI-DI 14250892903986 listed 19 Mar 2019 Listed
Timeline
- Cleared FDA 510(k) K072323
- Listed FDA GUDID 14250892903986
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Vyaire
- Generic name
- Cardiopulmonary stress exercise monitoring system
- Model / Ref / Catalog
- 707230
- Primary DI / UDI-DI
- 14250892903986
- 510(k) Number
- FDA product code
- BZC
- GMDN term
- Cardiopulmonary stress exercise monitoring system
- Device class
- Class II
- Regulation number
- 868.1880
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code BZC (Calculator, Pulmonary Function Data).
- OSCILLAIRE by JONES MEDICAL INSTRUMENT CO.
- PNEUMOSCREEN by Erich Jaeger GmbH
- SYSTEM 82 COMPUTERIZED LUNG VO. SPIRO by Pulmonary Testing Systems
- PULMONE MINIBOX PFT TM by Pulmone Advanced Medical Devices, Ltd.
- SPIROMETER MODEL TS-200 SLZ 7541 by Teledyne Avionics Div. of Teledyne
- BIORE CP-100 CARDIOPULMONARY MONITOR by Bicore Monitoring Systems
- Q-PLEX 1 by Quinton, Inc.
- VISTA INTERFACE SYSSTEM by Vacumetrics, Inc.
- PULMONARY FUNCTION TESTER, COMPUTERIZED by Warren E. Collins, Inc.
- SYSTEM 84 COMPUTERIZED LUNG VOL. SPIROM by Cardio Pulmonary Instruments