Barry J. Kaplan, Inc.
Country not established
- Devices
- 1
What Barry J. Kaplan, Inc. makes
Barry J. Kaplan, Inc. manufactures the MEGAVAC System, a medical device designed for vacuum-assisted wound closure and debridement.
The MEGAVAC System is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Megavac System Ref K974196
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Barry J. Kaplan, Inc. have in the registry?
The registry currently lists 1 device for Barry J. Kaplan, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Barry J. Kaplan, Inc.'s devices?
Among its 1 most recently registered device, Barry J. Kaplan, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Barry J. Kaplan, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Barry J. Kaplan, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Barry J. Kaplan, Inc. in the registry?
The most recently registered devices listed for Barry J. Kaplan, Inc. include MEGAVAC SYSTEM.