Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K151249Substantially Equivalent

Pureway Sharps Collector 1.2 Gallon, Pureway Sharps Collector 2 Gallon, Pureway Sharps Collector 3 Gallon

Pureway Compliance, Inc., Santa Monica CA / Traditional, Substantially Equivalent

K151249 is the FDA 510(k) clearance record for PUREWAY SHARPS COLLECTOR 1.2 GALLON, PUREWAY SHARPS COLLECTOR 2 GALLON, PUREWAY SHARPS COLLECTOR 3 GALLON, a class II device, cleared for Pureway Compliance, Inc. on under FDA product code MMK (Container, Sharps). FDA records list 3 510(k) clearances for Pureway Compliance, Inc., from to . As of , FDA records show no recalls naming K151249.

Clearance record

Decision date
Received
(115 days to decision)
Product code
MMK Container, Sharps
Regulation
21 CFR 880.5570
Device class
Class II
Review panel
General Hospital
Applicant
Pureway Compliance, Inc. 201 Santa Monica Blvd., Suite 400, Santa Monica CA
510(k) summary
Summary PDF
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