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FDA 510(k)

KOTEX LIGHTDAYS DEODORANT PANTILINERS

K-Number: K862285 · 1986-07-08

ApplicantKimberly-Clark Corp.
Decision Date1986-07-08
Product CodeHHL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KOTEX LIGHTDAYS DEODORANT PANTILINERS 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 1986-07-08 under 510(k) number K862285. 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 PANTILINERS?

KOTEX LIGHTDAYS DEODORANT PANTILINERS is a medical device that received FDA 510(k) clearance on 1986-07-08. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K862285.

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

KOTEX LIGHTDAYS DEODORANT PANTILINERS received FDA 510(k) clearance on 1986-07-08, under 510(k) number K862285.

Who is the listed applicant for KOTEX LIGHTDAYS DEODORANT PANTILINERS?

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 PANTILINERS?

The FDA product code for KOTEX LIGHTDAYS DEODORANT PANTILINERS 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.

K962954DEODORANT MAXI PADParagon Trade Brands, Inc.K962953DEODORANT PANTY SHIELDParagon Trade Brands, Inc.K962962DEODORANT PANTY LINERParagon 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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