510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K871672Substantially Equivalent

Sterilization Indicator for Flash Sterilization

Propper Mfg Co Inc, Long Island City NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K871672 is the FDA 510(k) clearance record for STERILIZATION INDICATOR FOR FLASH STERILIZATION, a class II device, cleared for Propper Mfg. Co., Inc. on under FDA product code LRT (Indicator, Sterilization). FDA records list 25 510(k) clearances for Propper Mfg. Co., Inc., from to . As of , FDA records show no recalls naming K871672.

Clearance record

Decision date
Received
(34 days to decision)
Product code
LRT Indicator, Sterilization
Regulation
21 CFR 880.2800
Device class
Class II
Review panel
General Hospital
Applicant
Propper Mfg. Co., Inc. 3604 Skillman Ave., Long Island City NY
Third party review
No

Clearances, product code LRT

Trailing 12 months

FDA records hold no clearances under product code LRT in the trailing twelve months.

FDA records show no clearances under product code LRT in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LRT, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260