Pgk, Inc.
Country not established
- Devices
- 1
What Pgk, Inc. makes
Pgk, Inc. manufactures the PGK Device (Modified), a Class I medical device designed for specific clinical applications.
The PGK Device (Modified) is regulated under the FDA’s 510(k) pathway and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Pgk Device (Modified) Ref K980997
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pgk, Inc. have in the registry?
The registry currently lists 1 device for Pgk, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pgk, Inc.'s devices?
Among its 1 most recently registered device, Pgk, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pgk, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pgk, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Pgk, Inc. in the registry?
The most recently registered devices listed for Pgk, Inc. include PGK DEVICE (MODIFIED).