Medical Device Manufacturer · US , Mchenry , IL

Premium Plastics, Inc. - FDA 510(k) Cleared Devices

9 submissions · 7 cleared · Since 1977

Total

Cleared

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

1-9 of 9

Cleared Aug 08, 1995

PULM O2 SUCTION CATHETER TRAYS

K953226 · BSY

Anesthesiology · 33d

Cleared Jun 21, 1995

GENT-L-KARE TRACHEOSTOMY TRAYS

K950851 · LRQ

General & Plastic Surgery · 117d

Cleared Mar 14, 1995

GENT-L-KARE LACERATION TRAYS

K950850 · FRG

General Hospital · 18d

Cleared Dec 14, 1994

ROLL-A-WAY SHARPS DISPOSAL SYSTEM (RED AND IVORY)

K943740 · FMI

General Hospital · 134d

Cleared Oct 24, 1989

GENT-L-KARE(TM) STERILE, PRESSURE SORE MANAGE KIT

K890107 · FRO

General & Plastic Surgery · 286d

Cleared Jun 22, 1989

GENT-L-KARE STER SUCT CATH TRAY W/14 FR/STER WATER

K893135 · JOL

General Hospital · 58d

Cleared Feb 28, 1985

GENT-L-KARE STERILE URETHRAL CATHETERIZATION TRAY

K850285 · KOD

Gastroenterology & Urology · 36d

Cleared Apr 29, 1980

STERILE SPONGE BOWLS

K800440 · FNY

General Hospital · 61d

Cleared Sep 06, 1977

STERILE SUTURE REMOVAL KIT

K771448 · KDD

General & Plastic Surgery · 35d

Premium Plastics, Inc. - FDA 510(k) Cleared Devices

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