Intera Shield and Intera Undergarment

FDA 510(k) K885185 · Intera Corp.

Substantially Equivalent

510(k) numberK885185

Submission

Device name
Intera Shield and Intera Undergarment
Applicant
Intera Corp.
Chattanooga, TN, US
Received
December 14, 1988
Decision date
February 8, 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
K891686Lib System, Baby/Adult DiaperEYQ · Traditional Intera Corp.05/31/1989SE
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
K891686Lib System, Baby/Adult DiaperEYQ · Traditional 05/31/1989SE
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 Intera Shield and Intera Undergarment cleared by the FDA?

Intera Shield and Intera Undergarment (K885185) received a 510(k) decision of Substantially Equivalent on February 8, 1989, 56 days after the submission was received.

What is the product code of K885185?

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