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FDA 510(k)

TAMPAX ULTRAFIT PANTY SHIELDS, DEODORANT

K-Number: K884951 · 1989-01-10

Decision Date1989-01-10
Product CodeHHL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TAMPAX ULTRAFIT PANTY SHIELDS, DEODORANT is the device name listed in this FDA 510(k) record. The listed applicant is Tambrands, Inc.. It received FDA 510(k) clearance on 1989-01-10 under 510(k) number K884951. The device is classified under product code HHL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TAMPAX ULTRAFIT PANTY SHIELDS, DEODORANT?

TAMPAX ULTRAFIT PANTY SHIELDS, DEODORANT is a medical device that received FDA 510(k) clearance on 1989-01-10. The listed applicant is Tambrands, Inc.. The 510(k) number is K884951.

When did TAMPAX ULTRAFIT PANTY SHIELDS, DEODORANT receive FDA 510(k) clearance?

TAMPAX ULTRAFIT PANTY SHIELDS, DEODORANT received FDA 510(k) clearance on 1989-01-10, under 510(k) number K884951.

Who is the listed applicant for TAMPAX ULTRAFIT PANTY SHIELDS, DEODORANT?

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 ULTRAFIT PANTY SHIELDS, DEODORANT?

The FDA product code for TAMPAX ULTRAFIT PANTY SHIELDS, DEODORANT is HHL.

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: HHL)

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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