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FDA 510(k)

TAMPAX COMPAK, COMPACT PLASTIC APPLI. REGU. TAMPON

K-Number: K880023 · 1988-03-02

Decision Date1988-03-02
Product CodeHIL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TAMPAX COMPAK, COMPACT PLASTIC APPLI. REGU. TAMPON is the device name listed in this FDA 510(k) record. The listed applicant is Tambrands, Inc.. It received FDA 510(k) clearance on 1988-03-02 under 510(k) number K880023. The device is classified under product code HIL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAMPAX COMPAK, COMPACT PLASTIC APPLI. REGU. TAMPON?

TAMPAX COMPAK, COMPACT PLASTIC APPLI. REGU. TAMPON is a medical device that received FDA 510(k) clearance on 1988-03-02. The listed applicant is Tambrands, Inc.. The 510(k) number is K880023.

When did TAMPAX COMPAK, COMPACT PLASTIC APPLI. REGU. TAMPON receive FDA 510(k) clearance?

TAMPAX COMPAK, COMPACT PLASTIC APPLI. REGU. TAMPON received FDA 510(k) clearance on 1988-03-02, under 510(k) number K880023.

Who is the listed applicant for TAMPAX COMPAK, COMPACT PLASTIC APPLI. REGU. TAMPON?

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 COMPAK, COMPACT PLASTIC APPLI. REGU. TAMPON?

The FDA product code for TAMPAX COMPAK, COMPACT PLASTIC APPLI. REGU. TAMPON is HIL.

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: HIL)

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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