Paul H. Schneider Ent.
Country not established
- Devices
- 1
What Paul H. Schneider Ent. makes
Paul H. Schneider Ent. manufactures the Kidd Vaginal Speculum, a medical device used in gynecological examinations to provide clear visualization of the vaginal canal and cervix.
The Kidd Vaginal Speculum 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
Kidd Vaginal Speculum Ref K841867
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Paul H. Schneider Ent. have in the registry?
The registry currently lists 1 device for Paul H. Schneider Ent.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Paul H. Schneider Ent.'s devices?
Among its 1 most recently registered device, Paul H. Schneider Ent. has devices listed in FDA 510(k) (1 device).
What risk classes do Paul H. Schneider Ent.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Paul H. Schneider Ent.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Paul H. Schneider Ent. in the registry?
The most recently registered devices listed for Paul H. Schneider Ent. include KIDD VAGINAL SPECULUM.