P.A. Research Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What P.A. Research Corp. makes
P.A. Research Corp. manufactures disposable patient examination gloves made from poly material and the Pullen Pocket Scope, a handheld optical device designed for medical examinations.
These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Patient Examination Gloves (Poly) Ref K892771
510(k) 510(k)Pullen Pocket Scope Ref K802818
510(k) 510(k)
Frequently asked questions
How many devices does P.A. Research Corp. have in the registry?
The registry currently lists 2 devices for P.A. Research Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list P.A. Research Corp.'s devices?
Among its 2 most recently registered devices, P.A. Research Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do P.A. Research Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for P.A. Research Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from P.A. Research Corp. in the registry?
The most recently registered devices listed for P.A. Research Corp. include PATIENT EXAMINATION GLOVES (POLY) and PULLEN POCKET SCOPE.