SCENTED MENSTRUAL PAD— 510(k) K844602

Name: FDA 510(k) clearance K844602
Creator: U.S. Food and Drug Administration
Published: 1985-01-16

Substantially Equivalent

Procter & Gamble Mfg. Co.

FDA 510(k) clearance K844602 for SCENTED MENSTRUAL PAD, Substantially Equivalent on 1985-01-16. 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: 1984-11-27
Decision date: 1985-01-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cincinnati, OH, US

Download summary PDF View on FDA.gov ↗

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

Data sourced from openFDA. This site is unofficial and independent of the FDA.