American Medical Devices, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
Catalogue
Moistair Fluid Air Tubing Set Ref K974561
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Endoview Spphire Lens Set Ref K971853
Regimes: 510(k) Registry: 510(k)Endosoft Soft Tip Needle (20 Ga. And 19 Ga.) Ref K970873
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Medical Devices, Inc. have in the registry?
The registry currently lists 6 devices for American Medical Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Medical Devices, Inc.'s devices?
Among its 6 most recently registered devices, American Medical Devices, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do American Medical Devices, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for American Medical Devices, 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 Medical Devices, Inc. in the registry?
The most recently registered devices listed for American Medical Devices, Inc. include MOISTAIR FLUID AIR TUBING SET, ENDOLIGHT FIBEROPTIC ENDO-ILLUMINATOR (20 GA. & 19 GA.), ENDOVIEW SPPHIRE LENS SET and ENDOSOFT SOFT TIP NEEDLE (20 GA. AND 19 GA.).