American Mammographics, Inc. is one of 25870 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Mammographics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: S.O.F.T. PADDLE (SPECIAL OPTIMIZED FULL COMPRESSION TRAY), MODEL SFT-PDLE, MAMMOSPOT PADDLE, AMI MAMMOSPOT
4
Total
4
Cleared
0
Denied
American Mammographics, Inc. has 4 FDA 510(k) cleared medical devices. Based in Chattanooga, US.
Historical record: 4 cleared submissions from 1990 to 2002. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by American Mammographics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Mammographics, Inc.
4 devices