510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K961156Substantially Equivalent

Once-a-Day Bowie and Dick Test Pack.

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

K961156 is the FDA 510(k) clearance record for ONCE-A-DAY BOWIE AND DICK TEST PACK., a class II device, cleared for Propper Mfg. Co., Inc. on under FDA product code JOJ (Indicator, Physical/Chemical Sterilization Process). FDA records list 25 510(k) clearances for Propper Mfg. Co., Inc., from to . As of , FDA records show no recalls naming K961156.

Clearance record

Decision date
Received
(375 days to decision)
Product code
JOJ Indicator, Physical/Chemical Sterilization Process
Regulation
21 CFR 880.2800
Device class
Class II
Review panel
General Hospital
Applicant
Propper Mfg. Co., Inc. 36-04 Skillman Ave., Long Island NY
510(k) summary
Statement
Third party review
No

Clearances, product code JOJ

Trailing 12 months
3 clearances under product code JOJ 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 JOJ, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20261
October 20260