SCENTED ALWAYS PANTILINERS— 510(k) K853000

Name: FDA 510(k) clearance K853000
Creator: U.S. Food and Drug Administration
Published: 1985-09-06

Substantially Equivalent

Procter & Gamble Mfg. Co.

FDA 510(k) clearance K853000 for SCENTED ALWAYS PANTILINERS, Substantially Equivalent on 1985-09-06. Applicant: Procter & Gamble Mfg. Co.. Device class: 2.

Clearance details

Applicant: Procter & Gamble Mfg. Co.
Product code: Code HHL
Device class: Class 2
Regulation: 21 CFR 884.5425
Advisory panel: Obstetrics/Gynecology
Date received: 1985-07-15
Decision date: 1985-09-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cincinnati, OH, US

Download summary PDF View on FDA.gov ↗

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K913237 — ALWAYS, SCENTED/SCENTED DEODORIZED MENSTRUAL PAD1991-09-23

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K864673 — UNSCENTED MENSTRUAL PAD1987-01-21
K861863 — MODIFIED PROTECTIVE GARMENT1986-08-11
K862348 — SINGLE-USE PATIENT UNDERPAD1986-07-02

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