Bca Biological Corp. of America
United StatesFDA applicant, unverified
- Devices
- 7
What Bca Biological Corp. of America makes
Bca Biological Corp. of America makes the RECAP device, which is classified as a Class II medical device.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
Freeze Dried Papain Ref K810803
Regimes: 510(k) Registry: 510(k)Elution Solution Ref K812565
Regimes: 510(k) Registry: 510(k)Em-V Ref K781397
Regimes: 510(k) Registry: 510(k)Hematology Control Ref K760162
Regimes: 510(k) Registry: 510(k)Freeze Dried Ficin Ref K813404
Regimes: 510(k) Registry: 510(k)Em-X Ref K812222
Regimes: 510(k) Registry: 510(k)Recap Ref K780665
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bca Biological Corp. of America have in the registry?
The registry currently lists 7 devices for Bca Biological Corp. of America. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bca Biological Corp. of America's devices?
Among its 7 most recently registered devices, Bca Biological Corp. of America has devices listed in FDA 510(k) (7 devices).
What risk classes do Bca Biological Corp. of America's devices fall under?
Among its 7 most recently registered devices, the classes recorded for Bca Biological Corp. of America's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bca Biological Corp. of America in the registry?
The most recently registered devices listed for Bca Biological Corp. of America include FREEZE DRIED PAPAIN, ELUTION SOLUTION, EM-V and HEMATOLOGY CONTROL.