American Health Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Patient Exam Gloves (Powder Free) Ref K923967
Regimes: 510(k) Registry: 510(k)Monitron System Ref K874148
Regimes: 510(k) Registry: 510(k)Patient Exam Gloves (Mfg. Multi-Com Sdn Bhd) Ref K892292
Regimes: 510(k) Registry: 510(k)Surgeon's Gloves Ref K974356
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Health Products, Inc. have in the registry?
The registry currently lists 5 devices for American Health Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Health Products, Inc.'s devices?
Among its 5 most recently registered devices, American Health Products, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do American Health Products, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for American Health Products, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Health Products, Inc. in the registry?
The most recently registered devices listed for American Health Products, Inc. include PATIENT EXAM GLOVES (MFG. AMERICAN RUBBER PRODUCT), PATIENT EXAM GLOVES (POWDER FREE), MONITRON SYSTEM and PATIENT EXAM GLOVES (MFG. MULTI-COM SDN BHD).