Jaeger 173115
by Jaeger Medical GmbH 3 variants
Jaeger 173115 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 04250892905051), 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 | Number04250892905051 | Date19 Mar 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK072323 | Date10 Oct 2007 | StatusActive |
Official records
- AccessGUDID record 04250892905051
- FDA 510(k) database K072323
Across registries
- FDA 510(k) K072323 decided 10 Oct 2007 Active
- FDA GUDID UDI-DI 04250892905051 listed 19 Mar 2019 Listed
Timeline
- Cleared FDA 510(k) K072323
- Listed FDA GUDID 04250892905051
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Jaeger
- Generic name
- Cardiopulmonary stress exercise monitoring system
- Model / Ref / Catalog
- 173115
- Primary DI / UDI-DI
- 04250892905051
- 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
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