SINGLE-USE PATIENT UNDERPAD— 510(k) K862348

Name: FDA 510(k) clearance K862348
Creator: U.S. Food and Drug Administration
Published: 1986-07-02

Substantially Equivalent

Procter & Gamble Mfg. Co.

FDA 510(k) clearance K862348 for SINGLE-USE PATIENT UNDERPAD, Substantially Equivalent on 1986-07-02. Applicant: Procter & Gamble Mfg. Co.. Device class: 1.

Clearance details

Applicant: Procter & Gamble Mfg. Co.
Product code: Code KME
Device class: Class 1
Regulation: 21 CFR 880.6060
Advisory panel: General Hospital
Date received: 1986-06-20
Decision date: 1986-07-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cincinnati, OH, US

Download summary PDF View on FDA.gov ↗

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K861863 — MODIFIED PROTECTIVE GARMENT1986-08-11
K860598 — MODIFIED PROTECTIVE GARMENT FOR INCONTINENTS1986-03-05

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