KOTEX SECURITY TUBE TAMPON
K-Number: K853192 · 1985-08-29
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Device Summary
Frequently Asked Questions
What is the KOTEX SECURITY TUBE TAMPON?
KOTEX SECURITY TUBE TAMPON is a medical device that received FDA 510(k) clearance on 1985-08-29. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K853192.
When did KOTEX SECURITY TUBE TAMPON receive FDA 510(k) clearance?
KOTEX SECURITY TUBE TAMPON received FDA 510(k) clearance on 1985-08-29, under 510(k) number K853192.
Who is the listed applicant for KOTEX SECURITY TUBE TAMPON?
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 TAMPON?
The FDA product code for KOTEX SECURITY TUBE TAMPON 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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