Preven-A-Stik, Inc.
Country not established
- Devices
- 1
What Preven-A-Stik, Inc. makes
Preven-A-Stik, Inc. manufactures the PREVEN-A-STIK, a medical device designed for wound protection and prevention of contamination in surgical and medical procedures.
The PREVEN-A-STIK is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Preven-A-Stik Ref K904148
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Preven-A-Stik, Inc. have in the registry?
The registry currently lists 1 device for Preven-A-Stik, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Preven-A-Stik, Inc.'s devices?
Among its 1 most recently registered device, Preven-A-Stik, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Preven-A-Stik, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Preven-A-Stik, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Preven-A-Stik, Inc. in the registry?
The most recently registered devices listed for Preven-A-Stik, Inc. include PREVEN-A-STIK.