Arthur F. Kozakowski, Jr.
Country not established
- Devices
- 1
What Arthur F. Kozakowski, Jr. makes
Arthur F. Kozakowski, Jr. manufactures glasses molasses, a Class I medical device used as a topical application for wound care or skin treatment.
The device is regulated under FDA 510(k) clearance as a Class I product and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Glasses Molasses Ref K930174
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arthur F. Kozakowski, Jr. have in the registry?
The registry currently lists 1 device for Arthur F. Kozakowski, Jr.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arthur F. Kozakowski, Jr.'s devices?
Among its 1 most recently registered device, Arthur F. Kozakowski, Jr. has devices listed in FDA 510(k) (1 device).
What risk classes do Arthur F. Kozakowski, Jr.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Arthur F. Kozakowski, Jr.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Arthur F. Kozakowski, Jr. in the registry?
The most recently registered devices listed for Arthur F. Kozakowski, Jr. include GLASSES MOLASSES.