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FDA 510(k)

KOTEX LIGHTDAYS LONGS DEODORANT & REG. PANTILINERS

K-Number: K882364 · 1988-08-02

ApplicantKimberly-Clark Corp.
Decision Date1988-08-02
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KOTEX LIGHTDAYS LONGS DEODORANT & REG. 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 1988-08-02 under 510(k) number K882364. The device is classified under product code HHD. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KOTEX LIGHTDAYS LONGS DEODORANT & REG. PANTILINERS?

KOTEX LIGHTDAYS LONGS DEODORANT & REG. PANTILINERS is a medical device that received FDA 510(k) clearance on 1988-08-02. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K882364.

When did KOTEX LIGHTDAYS LONGS DEODORANT & REG. PANTILINERS receive FDA 510(k) clearance?

KOTEX LIGHTDAYS LONGS DEODORANT & REG. PANTILINERS received FDA 510(k) clearance on 1988-08-02, under 510(k) number K882364.

Who is the listed applicant for KOTEX LIGHTDAYS LONGS DEODORANT & REG. 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 LONGS DEODORANT & REG. PANTILINERS?

The FDA product code for KOTEX LIGHTDAYS LONGS DEODORANT & REG. PANTILINERS is HHD.

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Other records listing Kimberly-Clark Corp. as applicant

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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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