510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K872313Substantially Equivalent

Needle & Blade Counter & Disposal Unit

Gary Plastic Packaging Corp., Bronx NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K872313 is the FDA 510(k) clearance record for NEEDLE & BLADE COUNTER & DISPOSAL UNIT, a class II device, cleared for Gary Plastic Packaging Corp. on under FDA product code MMK (Container, Sharps). FDA records list one 510(k) clearance for Gary Plastic Packaging Corp. As of , FDA records show no recalls naming K872313.

Clearance record

Decision date
Received
(15 days to decision)
Product code
MMK Container, Sharps
Regulation
21 CFR 880.5570
Device class
Class II
Review panel
General Hospital
Applicant
Gary Plastic Packaging Corp. 770 Garrison Ave., Bronx NY
Third party review
No

Clearances, product code MMK

Trailing 12 months
3 clearances under product code MMK in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code MMK, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20261
September 20260
October 20260