Bemis Mfg. Co. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
FDA 510(k) Regulatory Record - Bemis Mfg. Co. General Hospital ✕
12 devices
Cleared
Jul 11, 2002
NO-POKES NEEDLE SAFETY DEVICE
General Hospital
112d
Cleared
Feb 14, 1997
BEMIS TWO GALLON SHARPS CONTAINER
General Hospital
72d
Cleared
Feb 11, 1997
BEMIS TWO GALLON CHEMOTHERAPY CONTAINER
General Hospital
69d
Cleared
Mar 28, 1996
BEMIS ONE QUART PHLEBOTOMY CONTAINER (PART NUMBER 100)
General Hospital
52d
Cleared
Nov 27, 1995
SHARPS DISPOSAL CONTAINERS
General Hospital
108d
Cleared
Jun 02, 1995
IGHT AND ELEVEN GALLON SHARPS AND CHEMOTHERAPY CONTAINERS
General Hospital
126d
Cleared
May 23, 1994
SHARPS DISPOSABLE CONTAINERS
General Hospital
413d
Cleared
May 23, 1994
SHARP DISPOSAL CONTAINERS WALL SAFE
General Hospital
77d
Cleared
May 23, 1994
SHARPS DISPOSAL CONTAINER/PHLEBOTOMY
General Hospital
77d
Cleared
Feb 07, 1992
SUCTION CONNECTING TUBING
General Hospital
119d
Cleared
Jul 05, 1991
CHEMOTHERAPY CONTAINER
General Hospital
88d
Cleared
Sep 16, 1985
STERILIZATION CONTAINER
General Hospital
108d