Medical Corp. of America
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Phaco Packs, 1A Packs & Pack Components Ref K854116
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medical Corp. of America have in the registry?
The registry currently lists 4 devices for Medical Corp. of America. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Corp. of America's devices?
Among its 4 most recently registered devices, Medical Corp. of America has devices listed in FDA 510(k) (4 devices).
What risk classes do Medical Corp. of America's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Medical Corp. of America's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medical Corp. of America in the registry?
The most recently registered devices listed for Medical Corp. of America include TUBING A VIT, VIT, FRAG PACKS & NEEDLE & CLEAN WIR, KANSAS I/A SYSTEM & KANSAS I/A & VITRECTROMY SYST., PHACO PACKS, 1A PACKS & PACK COMPONENTS and DISPOSABLE ACCESSORIES FOR I/A SYS. & VITEOUS CUT..