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FDA 510(k)

KOTEX PROFILE SHAPED MAXI PAD

K-Number: K871210 · 1987-04-10

Decision Date1987-04-10
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KOTEX PROFILE SHAPED MAXI PAD 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 1987-04-10 under 510(k) number K871210. 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 PROFILE SHAPED MAXI PAD?

KOTEX PROFILE SHAPED MAXI PAD is a medical device that received FDA 510(k) clearance on 1987-04-10. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K871210.

When did KOTEX PROFILE SHAPED MAXI PAD receive FDA 510(k) clearance?

KOTEX PROFILE SHAPED MAXI PAD received FDA 510(k) clearance on 1987-04-10, under 510(k) number K871210.

Who is the listed applicant for KOTEX PROFILE SHAPED MAXI PAD?

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 PROFILE SHAPED MAXI PAD?

The FDA product code for KOTEX PROFILE SHAPED MAXI PAD is HHD.

Related Clinical Trials

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.

Other records listing Kimberly-Clark Corp. as applicant

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.

View all 102 devices →

Related Devices (Code: HHD)

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.

Official Source

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

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