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FDA 510(k)

TAMPAX CLOSED-END FLUSHABLE TAMPON, SUPER PLUS

K-Number: K870360 · 1987-02-25

Decision Date1987-02-25
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TAMPAX CLOSED-END FLUSHABLE TAMPON, SUPER PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Tambrands, Inc.. It received FDA 510(k) clearance on 1987-02-25 under 510(k) number K870360. 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 TAMPAX CLOSED-END FLUSHABLE TAMPON, SUPER PLUS?

TAMPAX CLOSED-END FLUSHABLE TAMPON, SUPER PLUS is a medical device that received FDA 510(k) clearance on 1987-02-25. The listed applicant is Tambrands, Inc.. The 510(k) number is K870360.

When did TAMPAX CLOSED-END FLUSHABLE TAMPON, SUPER PLUS receive FDA 510(k) clearance?

TAMPAX CLOSED-END FLUSHABLE TAMPON, SUPER PLUS received FDA 510(k) clearance on 1987-02-25, under 510(k) number K870360.

Who is the listed applicant for TAMPAX CLOSED-END FLUSHABLE TAMPON, SUPER PLUS?

The FDA 510(k) record lists Tambrands, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TAMPAX CLOSED-END FLUSHABLE TAMPON, SUPER PLUS?

The FDA product code for TAMPAX CLOSED-END FLUSHABLE TAMPON, SUPER PLUS 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 Tambrands, Inc. 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.

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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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