ClearanceBrief
Company ยท US

Premium Plastics, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1977 to 1995. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
BSYCatheters, Suction, Tracheobronchial1
FMINeedle, Hypodermic, Single Lumen1
FNYBasin, Emesis1
FRGWrap, Sterilization1
FRODressing, Wound, Drug1
JOLCatheter And Tip, Suction1
KDDKit, Surgical Instrument, Disposable1
KODCatheter, Urological1
LRQTracheostomy And Nasal Suctioning Kit1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 8, 1995K953226PULM O2 SUCTION CATHETER TRAYS
Premium Plastics, Inc.
BSY
Jun 21, 1995K950851GENT-L-KARE TRACHEOSTOMY TRAYS
Premium Plastics, Inc.
LRQ
Mar 14, 1995K950850GENT-L-KARE LACERATION TRAYS
Premium Plastics, Inc.
FRG
Dec 14, 1994K943740ROLL-A-WAY SHARPS DISPOSAL SYSTEM (RED AND IVORY)
Premium Plastics, Inc.
FMI
Oct 24, 1989K890107GENT-L-KARE(TM) STERILE, PRESSURE SORE MANAGE KIT
Premium Plastics, Inc.
FRO
Jun 22, 1989K893135GENT-L-KARE STER SUCT CATH TRAY W/14 FR/STER WATER
Premium Plastics, Inc.
JOL
Feb 28, 1985K850285GENT-L-KARE STERILE URETHRAL CATHETERIZATION TRAY
Premium Plastics, Inc.
KOD
Apr 29, 1980K800440STERILE SPONGE BOWLS
Premium Plastics, Inc.
FNY
Sep 6, 1977K771448STERILE SUTURE REMOVAL KIT
Premium Plastics, Inc.
KDD

Latest recalls

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