Ansley Medical Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ansley Medical Products, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Ansley Medical Products, Inc. has 5 FDA 510(k) cleared medical devices. Based in Dallas, US.
Historical record: 5 cleared submissions from 1992 to 1993. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ansley Medical Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ansley Medical Products, Inc.
5 devices
Cleared
Sep 13, 1993
ABDOMINAL FLUID CONTROL POUCH, 203-301-S
General Hospital
95d
Cleared
Jul 23, 1993
CATALOG NUMBER 111 (FACESHIELD)
General Hospital
275d
Cleared
Nov 23, 1992
RESTRAINT, PROTECTIVE N0. 103
General Hospital
75d
Cleared
Nov 23, 1992
FOLEY CATHETER TUBE HOLDER NO. 101
General Hospital
75d
Cleared
Nov 23, 1992
TUBE, LEAD, AND CORD HOLDER NO. 102
General Hospital
75d