Hougen Mfg., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Mini-Ciser Ref K974848
Regimes: 510(k) Registry: 510(k)X-Air-Ciser Ref K974849
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hougen Mfg., Inc. have in the registry?
The registry currently lists 2 devices for Hougen Mfg., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hougen Mfg., Inc.'s devices?
Among its 2 most recently registered devices, Hougen Mfg., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Hougen Mfg., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Hougen Mfg., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Hougen Mfg., Inc. in the registry?
The most recently registered devices listed for Hougen Mfg., Inc. include MINI-CISER and X-AIR-CISER.