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FDA 510(k)

KOTEX LIGHTDAYS DEODORANT PATILINERS

K-Number: K791433 · 1979-09-17

ApplicantKimberly-Clark Corp.
Decision Date1979-09-17
Product CodeHHL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KOTEX LIGHTDAYS DEODORANT PATILINERS is the device name listed in this FDA 510(k) record. The listed applicant is Kimberly-Clark Corp.. It received FDA 510(k) clearance on 1979-09-17 under 510(k) number K791433. The device is classified under product code HHL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KOTEX LIGHTDAYS DEODORANT PATILINERS?

KOTEX LIGHTDAYS DEODORANT PATILINERS is a medical device that received FDA 510(k) clearance on 1979-09-17. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K791433.

When did KOTEX LIGHTDAYS DEODORANT PATILINERS receive FDA 510(k) clearance?

KOTEX LIGHTDAYS DEODORANT PATILINERS received FDA 510(k) clearance on 1979-09-17, under 510(k) number K791433.

Who is the listed applicant for KOTEX LIGHTDAYS DEODORANT PATILINERS?

The FDA 510(k) record lists Kimberly-Clark Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KOTEX LIGHTDAYS DEODORANT PATILINERS?

The FDA product code for KOTEX LIGHTDAYS DEODORANT PATILINERS is HHL.

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Other records listing Kimberly-Clark Corp. as applicant

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Related Devices (Code: HHL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K962953DEODORANT PANTY SHIELDParagon Trade Brands, Inc.K962962DEODORANT PANTY LINERParagon Trade Brands, Inc.K962954DEODORANT MAXI PADParagon Trade Brands, Inc.K961119CAREFREE PANTYLINERSPersonal Products Co.K913238ALWAYS, UNSCENTED MENSTRUAL PADProcter & Gamble Co.K913237ALWAYS, SCENTED/SCENTED DEODORIZED MENSTRUAL PADProcter & Gamble Co.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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