Lib System, Baby/Adult Diaper

FDA 510(k) K891686 · Intera Corp.

Substantially Equivalent

510(k) numberK891686

Submission

Device name
Lib System, Baby/Adult Diaper
Applicant
Intera Corp.
Chattanooga, TN, US
Received
March 22, 1989
Decision date
May 31, 1989
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
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
K880455At Ease Adult DiaperEYQ · Traditional Hospital Specialty Co.04/14/1988SE

More from Hospital Specialty Co.

510(k)DeviceDecision
K885185Intera Shield and Intera UndergarmentEYQ · Traditional 02/08/1989SE
K883787Reusable Adult Incontinent DiaperEYQ · Traditional 11/07/1988SE
K883424Surgical Gown/Scrub/Laparotomy/Mayo Stand/Back TabKKX · Traditional 09/06/1988SE
K863732Surgical Drape & Drape AccessoriesKKX · Traditional 10/23/1986SE
K862380Mattress CoverEYQ · Traditional 07/28/1986SE

Questions and answers

When was Lib System, Baby/Adult Diaper cleared by the FDA?

Lib System, Baby/Adult Diaper (K891686) received a 510(k) decision of Substantially Equivalent on May 31, 1989, 70 days after the submission was received.

What is the product code of K891686?

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