KOTEX DISCRETE DIGITAL TAMPONS, REG.,SUPER,SUPER+
K-Number: K930149 · 1994-03-02
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Device Summary
Frequently Asked Questions
What is the KOTEX DISCRETE DIGITAL TAMPONS, REG.,SUPER,SUPER+?
KOTEX DISCRETE DIGITAL TAMPONS, REG.,SUPER,SUPER+ is a medical device that received FDA 510(k) clearance on 1994-03-02. The listed applicant is Kimberly-Clark Corp.. The 510(k) number is K930149.
When did KOTEX DISCRETE DIGITAL TAMPONS, REG.,SUPER,SUPER+ receive FDA 510(k) clearance?
KOTEX DISCRETE DIGITAL TAMPONS, REG.,SUPER,SUPER+ received FDA 510(k) clearance on 1994-03-02, under 510(k) number K930149.
Who is the listed applicant for KOTEX DISCRETE DIGITAL TAMPONS, REG.,SUPER,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 DISCRETE DIGITAL TAMPONS, REG.,SUPER,SUPER+?
The FDA product code for KOTEX DISCRETE DIGITAL TAMPONS, REG.,SUPER,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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