American Mammographics, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Mammospot Paddle Ref K954521
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Mammospot 3 And Mammospot 8 Ref K904517
Regimes: 510(k) Registry: 510(k)Ami Mammospot Ref K903651
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does American Mammographics, Inc. have in the registry?
The registry currently lists 4 devices for American Mammographics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list American Mammographics, Inc.'s devices?
Among its 4 most recently registered devices, American Mammographics, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do American Mammographics, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for American Mammographics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from American Mammographics, Inc. in the registry?
The most recently registered devices listed for American Mammographics, Inc. include MAMMOSPOT PADDLE, S.O.F.T. PADDLE (SPECIAL OPTIMIZED FULL COMPRESSION TRAY), MODEL SFT-PDLE, MAMMOSPOT 3 AND MAMMOSPOT 8 and AMI MAMMOSPOT.