SCENTED MENSTRUAL PAD— 510(k) K834131

Name: FDA 510(k) clearance K834131
Creator: U.S. Food and Drug Administration
Published: 1983-12-29

Substantially Equivalent

Procter & Gamble Mfg. Co.

FDA 510(k) clearance K834131 for SCENTED MENSTRUAL PAD, Substantially Equivalent on 1983-12-29. 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: 1983-12-01
Decision date: 1983-12-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HHL

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K962953 — DEODORANT PANTY SHIELD1996-10-10
K962954 — DEODORANT MAXI PAD1996-10-10
K962962 — DEODORANT PANTY LINER1996-10-10
K961119 — CAREFREE PANTYLINERS1996-04-17
K913237 — ALWAYS, SCENTED/SCENTED DEODORIZED MENSTRUAL PAD1991-09-23

More clearances from Procter & Gamble Mfg. Co.

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K873036 — ATTENDS INCONTINENT BRIEF1988-01-19
K873457 — SCENTED OR SCENTED DEODORIZED MENSTRUAL PADS1988-01-19
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.