C.F. Electronics, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 5
Catalogue
Drugbox Ref K955659
510(k) 510(k)Res Q Air System Model Ht-1000 Ref K926161
510(k) 510(k)Mark I Humidifier Ref K932570
510(k) 510(k)Hot Sack Ref K921395
510(k) 510(k)Therm O Drug Model Ht-747 Ref K922786
510(k) 510(k)
Frequently asked questions
How many devices does C.F. Electronics, Inc. have in the registry?
The registry currently lists 5 devices for C.F. Electronics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list C.F. Electronics, Inc.'s devices?
Among its 5 most recently registered devices, C.F. Electronics, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do C.F. Electronics, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for C.F. Electronics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from C.F. Electronics, Inc. in the registry?
The most recently registered devices listed for C.F. Electronics, Inc. include DRUGBOX, RES Q AIR SYSTEM MODEL HT-1000, MARK I HUMIDIFIER and HOT SACK.