510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K792629Substantially Equivalent

Sterilization Process/t-Binder

Procter & Gamble Mfg. Co., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K792629 is the FDA 510(k) clearance record for STERILIZATION PROCESS/T-BINDER, a class I device, cleared for Procter & Gamble Mfg. Co. on under FDA product code KMO (Binder, Elastic). FDA records list 72 510(k) clearances for Procter & Gamble Mfg. Co., from to . As of , FDA records show no recalls naming K792629.

Clearance record

Decision date
Received
(23 days to decision)
Product code
KMO Binder, Elastic
Regulation
21 CFR 880.5160
Device class
Class I
Review panel
General Hospital
Applicant
Procter & Gamble Mfg. Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KMO

Trailing 12 months

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

FDA records show no clearances under product code KMO in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KMO, 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