Cleared Traditional

K850611 - ATTENDS INCONTINENT UNDERGARMENT
(FDA 510(k) Clearance)

Feb 1985
Decision
11d
Days
Class 1
Risk

K850611 is an FDA 510(k) clearance for the ATTENDS INCONTINENT UNDERGARMENT. This device is classified as a Garment, Protective, For Incontinence (Class I - General Controls, product code EYQ).

Submitted by Procter & Gamble Mfg. Co. (Cincinnati, US). The FDA issued a Cleared decision on February 26, 1985, 11 days after receiving the submission on February 15, 1985.

This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5920.

Submission Details

510(k) Number K850611 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 15, 1985
Decision Date February 26, 1985
Days to Decision 11 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary

Device Classification

Product Code EYQ — Garment, Protective, For Incontinence
Device Class Class I - General Controls
CFR Regulation 21 CFR 876.5920

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