Bemis Mfg. Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bemis Mfg. Co. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Bemis Mfg. Co. has 12 FDA 510(k) cleared general hospital devices. Based in Sheboygan Falls, US.
Historical record: 12 cleared submissions from 1985 to 2002.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bemis Mfg. Co.
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