Klein-Baker Medical, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Klein-Baker Medical, Inc. has 5 FDA 510(k) cleared medical devices. Based in San Antonio, US.
Historical record: 5 cleared submissions from 1996 to 1997. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Klein-Baker Medical, Inc. Filter by specialty or product code using the sidebar.
5 devices
Cleared
Sep 29, 1997
NEO-CARE PERITONEAL DIALYSIS ADMINISTRATION SET
Gastroenterology & Urology
69d
Cleared
May 22, 1997
NEO-CARE LUMBER PUNCTURE KIT
Anesthesiology
64d
Cleared
Apr 01, 1997
NEO-PICC
General Hospital
55d
Cleared
Dec 24, 1996
NEO-CARE DUAL LUMEN UMBILICAL CATHETER
General Hospital
82d
Cleared
Nov 06, 1996
NEO-CARE CATHETERIZATION TRAY
General Hospital
41d