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FDA 510(k)

KOTEX OVERNITE

K-Number: K860587 · 1986-03-13

ApplicantKimberly-Clark Corp.
Decision Date1986-03-13
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KOTEX OVERNITE 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 1986-03-13 under 510(k) number K860587. 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 OVERNITE?

KOTEX OVERNITE is a medical device that received FDA 510(k) clearance on 1986-03-13. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K860587.

When did KOTEX OVERNITE receive FDA 510(k) clearance?

KOTEX OVERNITE received FDA 510(k) clearance on 1986-03-13, under 510(k) number K860587.

Who is the listed applicant for KOTEX OVERNITE?

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 OVERNITE?

The FDA product code for KOTEX OVERNITE 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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