American Medical Technology, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Choice Powered Wheelchair Ref K963808
Regimes: 510(k) Registry: 510(k)Surgical Drape Ref K873313
Regimes: 510(k) Registry: 510(k)Plastic Tubing Connector Ref K874360
Regimes: 510(k) Registry: 510(k)Needle Container Ref K874430
Regimes: 510(k) Registry: 510(k)Ametec Masy Modular Angioscope System Ref K905745
Regimes: 510(k) Registry: 510(k)Resuscitator Ref K874567
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Medical Technology, Inc. have in the registry?
The registry currently lists 6 devices for American Medical Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Medical Technology, Inc.'s devices?
Among its 6 most recently registered devices, American Medical Technology, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do American Medical Technology, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for American Medical Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Medical Technology, Inc. in the registry?
The most recently registered devices listed for American Medical Technology, Inc. include CHOICE POWERED WHEELCHAIR, SURGICAL DRAPE, PLASTIC TUBING CONNECTOR and NEEDLE CONTAINER.