510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K782112Substantially Equivalent

Pads, Mini, Maxi

Intl. Playtex, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K782112 is the FDA 510(k) clearance record for PADS, MINI, MAXI, a class I device, cleared for Intl. Playtex, Inc. 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 10 510(k) clearances for Intl. Playtex, Inc., from to . As of , FDA records show no recalls naming K782112.

Clearance record

Decision date
Received
(21 days to decision)
Product code
HHD Pad, Menstrual, Unscented
Regulation
21 CFR 884.5435
Device class
Class I
Review panel
Obstetrics/Gynecology
Applicant
Intl. Playtex, Inc. 4221 Richmond Rd., NW, Walker MI
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