Hoffman Laboratories, LLC
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Breathex Omega Cpap Device, Model 322 Ref K052597
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hoffman Laboratories, LLC have in the registry?
The registry currently lists 2 devices for Hoffman Laboratories, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hoffman Laboratories, LLC's devices?
Among its 2 most recently registered devices, Hoffman Laboratories, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Hoffman Laboratories, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hoffman Laboratories, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hoffman Laboratories, LLC in the registry?
The most recently registered devices listed for Hoffman Laboratories, LLC include BREATHX NASAL PILLOW AND MASK SYSTEM, MODEL 011-0003 and BREATHEX OMEGA CPAP DEVICE, MODEL 322.