Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

KOTEX STICK TAMPONS, REGULAR AND SUPER

K-Number: K872018 · 1987-06-24

Decision Date1987-06-24
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KOTEX STICK TAMPONS, REGULAR AND SUPER 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 1987-06-24 under 510(k) number K872018. 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 STICK TAMPONS, REGULAR AND SUPER?

KOTEX STICK TAMPONS, REGULAR AND SUPER is a medical device that received FDA 510(k) clearance on 1987-06-24. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K872018.

When did KOTEX STICK TAMPONS, REGULAR AND SUPER receive FDA 510(k) clearance?

KOTEX STICK TAMPONS, REGULAR AND SUPER received FDA 510(k) clearance on 1987-06-24, under 510(k) number K872018.

Who is the listed applicant for KOTEX STICK TAMPONS, REGULAR AND SUPER?

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 STICK TAMPONS, REGULAR AND SUPER?

The FDA product code for KOTEX STICK TAMPONS, REGULAR AND SUPER 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

View on FDA Database →

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

↑