Cleared Traditional

K883787 - REUSABLE ADULT INCONTINENT DIAPER

K883787 is an FDA 510(k) clearance for REUSABLE ADULT INCONTINENT DIAPER, manufactured by Intera Corp.. The device is a Class 1 Gastroenterology & Urology device with product code EYQ cleared through the Traditional 510(k) pathway after a 61-day FDA review.

K883787 · Intera Corp. · Gastroenterology & Urology device
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Nov 1988
Decision
61d
Days
Class 1
Risk

K883787 is an FDA 510(k) clearance for the REUSABLE ADULT INCONTINENT DIAPER. Classified as Garment, Protective, For Incontinence (product code EYQ), Class I - General Controls.

Submitted by Intera Corp. (Chattanooga, US). The FDA issued a Cleared decision on November 7, 1988 after a review of 61 days - a notably fast clearance cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5920 - the FDA gastroenterology and urology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Intera Corp. devices

FDA 510(k) Submission Details - K883787

510(k) Number K883787 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 07, 1988
Decision Date November 07, 1988
Days to Decision 61 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
69d faster than avg
Panel avg: 130d · This submission: 61d
Pathway characteristics
Predicate-based equivalence.

EYQ Device Classification - Class 1, General Controls

Product Code EYQ Garment, Protective, For Incontinence
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 876.5920
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - EYQ Garment, Protective, For Incontinence

All 16
Devices cleared under the same product code (EYQ) and FDA review panel - the closest regulatory comparables to K883787.
ATTENDS INCONTINENT BRIEF
K873036 · Procter & Gamble Mfg. Co. · Jan 1988
MALE URINARY STRESS PAD*
K862877 · Convatec, A Division of E.R. Squibb & Sons · Nov 1986
FREE & ACTIVE(TM) ABSORBENT PADS
K862878 · Convatec, A Division of E.R. Squibb & Sons · Nov 1986
MODIFIED PROTECTIVE GARMENT
K861863 · Procter & Gamble Mfg. Co. · Aug 1986
MODIFIED PROTECTIVE GARMENT FOR INCONTINENTS
K860598 · Procter & Gamble Mfg. Co. · Mar 1986
DEPEND FITTED BRIEF
K854378 · Kimberly-Clark Corp. · Dec 1985