Jay-Y Enterprises Co., Inc.
Country not established
- Devices
- 1
What Jay-Y Enterprises Co., Inc. makes
Jay-Y Enterprises Co., Inc. manufactures Class I medical devices, including non-generic products designed for specific clinical applications.
The company’s portfolio is regulated under the FDA’s 510(k) clearance process and is listed in the U.S. regulatory database. The manufacturer operates from the United States.
Catalogue
None-Generic Ref K940726
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Jay-Y Enterprises Co., Inc. have in the registry?
The registry currently lists 1 device for Jay-Y Enterprises Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jay-Y Enterprises Co., Inc.'s devices?
Among its 1 most recently registered device, Jay-Y Enterprises Co., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Jay-Y Enterprises Co., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Jay-Y Enterprises Co., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Jay-Y Enterprises Co., Inc. in the registry?
The most recently registered devices listed for Jay-Y Enterprises Co., Inc. include NONE-GENERIC.