Bionomy, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bionomy, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Bionomy, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1981 to 1985. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Bionomy, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bionomy, Inc.
5 devices
Cleared
Apr 12, 1985
BIONOMY'S MULTI-LUMEN CENTRAL VENOUS CATHETER-SET
General Hospital
24d
Cleared
Nov 29, 1984
PRUITT IRRIGATION AND OCCLUSION CATHETER
General & Plastic Surgery
42d
Cleared
Aug 31, 1983
EMBOLECTOMY CATHETER
Cardiovascular
79d
Cleared
Nov 16, 1981
PRUITT ARTERIAL OCCLUSION CHOLANG. CATH
Cardiovascular
112d
Cleared
Jun 30, 1981
OCCLUSION CATHETER
Cardiovascular
53d