510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K850955Substantially Equivalent

Always Maxipads - Unscented

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

K850955 is the FDA 510(k) clearance record for ALWAYS MAXIPADS - UNSCENTED, a class I device, cleared for Procter & Gamble Mfg. Co. on under FDA product code HHD (Pad, Menstrual, Unscented). FDA's definition for product code HHD reads: "An unscented menstrual pad which is used to absorb menstrual fluid or other vaginal discharge and is made of common cellulosic and synthetic material with an established safety profile". FDA records list 72 510(k) clearances for Procter & Gamble Mfg. Co., from to . As of , FDA records show no recalls naming K850955.

Clearance record

Decision date
Received
(67 days to decision)
Product code
HHD Pad, Menstrual, Unscented
Regulation
21 CFR 884.5435
Device class
Class I
Review panel
Obstetrics/Gynecology
Applicant
Procter & Gamble Mfg. Co. P.O. Box 599, Cincinnati OH
Third party review
No

Clearances, product code HHD

Trailing 12 months

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

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