American Biosurgical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Biosurgical, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
American Biosurgical, Inc. has 3 FDA 510(k) cleared medical devices. Based in Norcross, US.
Historical record: 3 cleared submissions from 1995 to 1997. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by American Biosurgical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Biosurgical, Inc.
3 devices
Cleared
Sep 19, 1997
AMERICAN BIOSURGICAL ELECTROSURGICAL BIPOLAR CABLE/CORD
General & Plastic Surgery
44d
Cleared
Aug 14, 1997
AMERICAN BIOSURGICAL ELECTROSURGICAL MONOPOLAR CABLE/CORD
General & Plastic Surgery
108d
Cleared
Oct 18, 1995
AMERICAN BIOSURGICAL ELECTROSURGICAL BIPOLAR CABLE/CORD
General & Plastic Surgery
62d