Premium Plastics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Premium Plastics, Inc. - FDA 510(k) Cleared Devices
9
Total
7
Cleared
0
Denied
Premium Plastics, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1977 to 1995. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Premium Plastics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Premium Plastics, Inc.
9 devices
Cleared
Aug 08, 1995
PULM O2 SUCTION CATHETER TRAYS
Anesthesiology
33d
Cleared
Jun 21, 1995
GENT-L-KARE TRACHEOSTOMY TRAYS
General & Plastic Surgery
117d
Cleared
Mar 14, 1995
GENT-L-KARE LACERATION TRAYS
General Hospital
18d
Cleared
Dec 14, 1994
ROLL-A-WAY SHARPS DISPOSAL SYSTEM (RED AND IVORY)
General Hospital
134d
Cleared
Oct 24, 1989
GENT-L-KARE(TM) STERILE, PRESSURE SORE MANAGE KIT
General & Plastic Surgery
286d
Cleared
Jun 22, 1989
GENT-L-KARE STER SUCT CATH TRAY W/14 FR/STER WATER
General Hospital
58d
Cleared
Feb 28, 1985
GENT-L-KARE STERILE URETHRAL CATHETERIZATION TRAY
Gastroenterology & Urology
36d
Cleared
Apr 29, 1980
STERILE SPONGE BOWLS
General Hospital
61d
Cleared
Sep 06, 1977
STERILE SUTURE REMOVAL KIT
General & Plastic Surgery
35d