Baka Manufacturing Co., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Catheter Strap & Ruinary Bay Holder Ref K780190
Regimes: 510(k) Registry: 510(k)Grip, Hospital Utility Ref K781800
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Baka Manufacturing Co., Inc. have in the registry?
The registry currently lists 2 devices for Baka Manufacturing Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Baka Manufacturing Co., Inc.'s devices?
Among its 2 most recently registered devices, Baka Manufacturing Co., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Baka Manufacturing Co., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Baka Manufacturing Co., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Baka Manufacturing Co., Inc. in the registry?
The most recently registered devices listed for Baka Manufacturing Co., Inc. include CATHETER STRAP & RUINARY BAY HOLDER and GRIP, HOSPITAL UTILITY.