Cleared Traditional

K845010 - CHESEBROUGH-POND'S URI-DRAIN MALE URINA...

K845010 is the FDA 510(k) clearance for CHESEBROUGH-POND'S URI-DRAIN MALE URINA... by Chesebrough-Pond'S U.S.A. Co.. It is a Class 1 Gastroenterology & Urology device (product code EYQ) cleared through the Traditional 510(k) pathway after a 20-day FDA review.

K845010 · Chesebrough-Pond'S U.S.A. Co. · Gastroenterology & Urology device
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Jan 1985
Decision
20d
Days
Class 1
Risk

K845010 is an FDA 510(k) clearance for the CHESEBROUGH-POND'S URI-DRAIN MALE URINARY POUCH. Classified as Garment, Protective, For Incontinence (product code EYQ), Class I - General Controls.

Submitted by Chesebrough-Pond'S U.S.A. Co. (Trumbull, US). The FDA issued a Cleared decision on January 15, 1985 after a review of 20 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 Chesebrough-Pond'S U.S.A. Co. devices

Submission Details

510(k) Number K845010 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 26, 1984
Decision Date January 15, 1985
Days to Decision 20 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
110d faster than avg
Panel avg: 130d · This submission: 20d
Pathway characteristics
Predicate-based equivalence.

Device Classification

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 14
Devices cleared under the same product code (EYQ) and FDA review panel - the closest regulatory comparables to K845010.
ATTENDS INCONTINENT UNDERGARMENT
K850611 · Procter & Gamble Mfg. Co. · Feb 1985
ADULT DISPOS. INCONTINENT PANTS
K850153 · Convatec, A Division of E.R. Squibb & Sons · Feb 1985
DIGNITY PANT & ABSORBENT PADS
K850154 · Convatec, A Division of E.R. Squibb & Sons · Feb 1985
ADULT INCONTINENCE PAD
K834295 · Procter & Gamble Mfg. Co. · Feb 1984
ADULT INCONTINENCE BRIEF
K834296 · Procter & Gamble Mfg. Co. · Feb 1984
ADULT INCONTINET BRIEF
K821397 · Johnson & Johnson Professionals, Inc. · May 1982