ALWAYS MAXIPADS - UNSCENTED— 510(k) K850955

Name: FDA 510(k) clearance K850955
Creator: U.S. Food and Drug Administration
Published: 1985-05-14

Substantially Equivalent

Procter & Gamble Mfg. Co.

FDA 510(k) clearance K850955 for ALWAYS MAXIPADS - UNSCENTED, Substantially Equivalent on 1985-05-14. Applicant: Procter & Gamble Mfg. Co.. Device class: 1.

Clearance details

Applicant: Procter & Gamble Mfg. Co.
Product code: Code HHD
Device class: Class 1
Regulation: 21 CFR 884.5435
Advisory panel: Obstetrics/Gynecology
Date received: 1985-03-08
Decision date: 1985-05-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cincinnati, OH, US

Download summary PDF View on FDA.gov ↗

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