Dripride Provide Ultra

FDA 510(k) K872059 · Weyerhaeuser Co.

Substantially Equivalent

510(k) numberK872059

Submission

Device name
Dripride Provide Ultra
Applicant
Weyerhaeuser Co.
Tacoma, WA, US
Received
May 28, 1987
Decision date
March 16, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
EYQ – Garment, Protective, For Incontinence
Device class
Class I (low risk)
Regulation
21 CFR 876.5920
Specialty
Gastroenterology, Urology

Other 510(k)s with product code EYQ

510(k)DeviceApplicantDecision
K950784Dristar Urinary Incontinence Management SystemEYQ · Traditional Advanced Bioresearch Assoc.05/03/1995SE
K932310Kit Pak Incontinent Skin Care KitEYQ · Traditional Kit Pak, Inc.06/01/1994SEKD
K903342Deodorizing and Sound Muffling Anal PadEYQ · Traditional Biological Resistance, Inc.10/23/1990SE
K891686Lib System, Baby/Adult DiaperEYQ · Traditional Intera Corp.05/31/1989SE
K885185Intera Shield and Intera UndergarmentEYQ · Traditional Intera Corp.02/08/1989SE
K883895Dripride Ultra Incontinent PadEYQ · Traditional Weyerhaeuser Co.01/30/1989SE
K883894Dripride Provide SlimEYQ · Traditional Weyerhaeuser Co.01/30/1989SE
K883787Reusable Adult Incontinent DiaperEYQ · Traditional Intera Corp.11/07/1988SE
K882418Dry Comfort UndergarmentEYQ · Traditional Health Tec, Inc.09/29/1988SE
K880454At Ease Stress PadEYQ · Traditional Hospital Specialty Co.06/16/1988SE

More from Hospital Specialty Co.

510(k)DeviceDecision
K883895Dripride Ultra Incontinent PadEYQ · Traditional 01/30/1989SE
K883894Dripride Provide SlimEYQ · Traditional 01/30/1989SE
K881859Dripride Disposable UnderpadKME · Traditional 06/03/1988SE
K871725Dripride Disposable UnderpadsKME · Traditional 05/15/1987SE
K854408Adult Absorbent Incontinent BriefEYQ · Traditional 11/19/1985SE
K834359Absorbent Incontinent Pads & BriefsEYQ · Traditional 03/05/1984SE
K831593Maxi ShieldsHHD · Traditional 08/12/1983SE
K830224Unscented Panty ShieldsHHD · Traditional 02/08/1983SE
K812577Unscented Menstrual PadsHHD · Traditional 10/19/1981SE

Questions and answers

When was Dripride Provide Ultra cleared by the FDA?

Dripride Provide Ultra (K872059) received a 510(k) decision of Substantially Equivalent on March 16, 1988, 293 days after the submission was received.

What is the product code of K872059?

The FDA product code is EYQ – Garment, Protective, For Incontinence, a Class I (low risk) device regulated under 21 CFR 876.5920.