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
K883895Substantially Equivalent

Dripride Ultra Incontinent Pad

Weyerhaeuser Co., Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K883895 is the FDA 510(k) clearance record for DRIPRIDE ULTRA INCONTINENT PAD, a class I device, cleared for Weyerhaeuser Co. on under FDA product code EYQ (Garment, Protective, For Incontinence). FDA records list 10 510(k) clearances for Weyerhaeuser Co., from to . As of , FDA records show no recalls naming K883895.

Clearance record

Decision date
Received
(138 days to decision)
Product code
EYQ Garment, Protective, For Incontinence
Regulation
21 CFR 876.5920
Device class
Class I
Review panel
Gastroenterology, Urology
Applicant
Weyerhaeuser Co. 2101 L St. NW, Washington DC
Third party review
No

Clearances, product code EYQ

Trailing 12 months

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

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