American Theracare is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Theracare - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
American Theracare has 1 FDA 510(k) cleared medical devices. Based in Garden Grove, US.
Historical record: 1 cleared submissions from 1986 to 1986. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by American Theracare Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Theracare
1 devices