Sabratek Corp. - FDA 510(k) Cleared Devices
Recent clearances: SABRATEK 4040 INFUSION PUMP, SABRATEK PATIENT HOME MANAGEMENT SYSTEM
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Sabratek Corp. General Hospital ✕
6 devices
Cleared
Mar 12, 1999
SABRATEK APM-2000 AMBULATORY PATIENT MONTOR, TRANSCUTANEOUS TEMPERATURE MONITOR
General Hospital
170d
Cleared
Feb 24, 1999
SABRATEK 4040 INFUSION PUMP
General Hospital
363d
Cleared
Jun 03, 1996
3030 INFUSION PUMP
General Hospital
200d
Cleared
Mar 23, 1995
SABRATEK SABSIL SETS
General Hospital
202d
Cleared
Jul 19, 1994
SABRATEK 6060 HOMERUN VOLUMETRIC INFUSION PUMP
General Hospital
85d
Cleared
May 18, 1992
SABRATEK 3030 INFUSION PUMP
General Hospital
215d