Lifepoint, Inc
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Cpr Locator Ref K833737
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lifepoint, Inc have in the registry?
The registry currently lists 3 devices for Lifepoint, Inc. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lifepoint, Inc's devices?
Among its 3 most recently registered devices, Lifepoint, Inc has devices listed in FDA 510(k) (3 devices).
What risk classes do Lifepoint, Inc's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Lifepoint, Inc's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lifepoint, Inc in the registry?
The most recently registered devices listed for Lifepoint, Inc include IMPACT TEST SYSTEM; SALIVA TEST MODULE-OPIATE (PRESCRIPTION USE), IMPACT TEST SYSTEM SALIVA TEST MODULE-OPIATE (WORKPLACE) and CPR LOCATOR.