Prolax Medical Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Prolax Disposable Latex Gloves (Examination) Ref K903352
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Prolax Medical Products, Inc. have in the registry?
The registry currently lists 3 devices for Prolax Medical Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Prolax Medical Products, Inc.'s devices?
Among its 3 most recently registered devices, Prolax Medical Products, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Prolax Medical Products, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Prolax Medical Products, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Prolax Medical Products, Inc. in the registry?
The most recently registered devices listed for Prolax Medical Products, Inc. include PROLAX DISPOSABLE LATEX GLOVES (PROCEDURE STERILE), PROLAX DISPOSABLE LATEX GLOVES (EXAM) HYPOALLERGEN and PROLAX DISPOSABLE LATEX GLOVES (EXAMINATION).