510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K924502Substantially Equivalent

Reusable Menstrual Pad

Keema and Co., Brier WA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K924502 is the FDA 510(k) clearance record for REUSABLE MENSTRUAL PAD, a class I device, cleared for Keema and 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 one 510(k) clearance for Keema and Co. As of , FDA records show no recalls naming K924502.

Clearance record

Decision date
Received
(817 days to decision)
Product code
HHD Pad, Menstrual, Unscented
Regulation
21 CFR 884.5435
Device class
Class I
Review panel
Obstetrics/Gynecology
Applicant
Keema and Co. 2429 236th St. SW, Brier WA
510(k) summary
Statement
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