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FDA 510(k)

KOTEX SECURITY TUBE TAMPONS

K-Number: K885194 · 1989-03-01

Decision Date1989-03-01
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KOTEX SECURITY TUBE TAMPONS 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 1989-03-01 under 510(k) number K885194. The device is classified under product code HEB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KOTEX SECURITY TUBE TAMPONS?

KOTEX SECURITY TUBE TAMPONS is a medical device that received FDA 510(k) clearance on 1989-03-01. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K885194.

When did KOTEX SECURITY TUBE TAMPONS receive FDA 510(k) clearance?

KOTEX SECURITY TUBE TAMPONS received FDA 510(k) clearance on 1989-03-01, under 510(k) number K885194.

Who is the listed applicant for KOTEX SECURITY TUBE TAMPONS?

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 SECURITY TUBE TAMPONS?

The FDA product code for KOTEX SECURITY TUBE TAMPONS is HEB.

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: HEB)

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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