Comform Absorbant Incontinence Pads

FDA 510(k) K781375 · Kimberly-Clark Corp.

Substantially Equivalent

510(k) numberK781375

Submission

Device name
Comform Absorbant Incontinence Pads
Applicant
Kimberly-Clark Corp.
Walker, MI, US
Received
August 9, 1978
Decision date
September 20, 1978
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

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Questions and answers

When was Comform Absorbant Incontinence Pads cleared by the FDA?

Comform Absorbant Incontinence Pads (K781375) received a 510(k) decision of Substantially Equivalent on September 20, 1978, 42 days after the submission was received.

What is the product code of K781375?

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