KOTEX SECURITY TAMPONS, REGULAR AND SUPER
K-Number: K864750 · 1987-01-28
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Device Summary
Frequently Asked Questions
What is the KOTEX SECURITY TAMPONS, REGULAR AND SUPER?
KOTEX SECURITY TAMPONS, REGULAR AND SUPER is a medical device that received FDA 510(k) clearance on 1987-01-28. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K864750.
When did KOTEX SECURITY TAMPONS, REGULAR AND SUPER receive FDA 510(k) clearance?
KOTEX SECURITY TAMPONS, REGULAR AND SUPER received FDA 510(k) clearance on 1987-01-28, under 510(k) number K864750.
Who is the listed applicant for KOTEX SECURITY 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 SECURITY TAMPONS, REGULAR AND SUPER?
The FDA product code for KOTEX SECURITY 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.
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.
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