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FDA 510(k)

KOTEX DISCRETE DIGITAL TAMPONS, REG.,SUPER,SUPER+

K-Number: K930149 · 1994-03-02

Decision Date1994-03-02
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KOTEX DISCRETE DIGITAL TAMPONS, REG.,SUPER,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 1994-03-02 under 510(k) number K930149. 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 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.

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

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

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