KOTEX SECURITY TUBE TAMPONS
K-Number: K802193 · 1980-11-12
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Device Summary
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 1980-11-12. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K802193.
When did KOTEX SECURITY TUBE TAMPONS receive FDA 510(k) clearance?
KOTEX SECURITY TUBE TAMPONS received FDA 510(k) clearance on 1980-11-12, under 510(k) number K802193.
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.
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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