KOTEX LIGHTDAYS DEODORANT PATILINERS— 510(k) K791433

Name: FDA 510(k) clearance K791433
Creator: U.S. Food and Drug Administration
Published: 1979-09-17

Substantially Equivalent

Kimberly-Clark Corp.

FDA 510(k) clearance K791433 for KOTEX LIGHTDAYS DEODORANT PATILINERS, Substantially Equivalent on 1979-09-17. Applicant: Kimberly-Clark Corp.. Device class: 2.

Clearance details

Applicant: Kimberly-Clark Corp.
Product code: Code HHL
Device class: Class 2
Regulation: 21 CFR 884.5425
Advisory panel: Obstetrics/Gynecology
Date received: 1979-07-27
Decision date: 1979-09-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K961119 — CAREFREE PANTYLINERS1996-04-17
K913237 — ALWAYS, SCENTED/SCENTED DEODORIZED MENSTRUAL PAD1991-09-23

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