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FDA 510(k)

FEMTEX AND PRIVATE LABEL SCENTED PLASTIC APPLICATOR TAMPONS

K-Number: K032173 · 2003-09-03

Decision Date2003-09-03
Product CodeHIL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FEMTEX AND PRIVATE LABEL SCENTED PLASTIC APPLICATOR TAMPONS is the device name listed in this FDA 510(k) record. The listed applicant is First Quality Hygienic, Inc.. It received FDA 510(k) clearance on 2003-09-03 under 510(k) number K032173. 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 FEMTEX AND PRIVATE LABEL SCENTED PLASTIC APPLICATOR TAMPONS?

FEMTEX AND PRIVATE LABEL SCENTED PLASTIC APPLICATOR TAMPONS is a medical device that received FDA 510(k) clearance on 2003-09-03. The listed applicant is First Quality Hygienic, Inc.. The 510(k) number is K032173.

When did FEMTEX AND PRIVATE LABEL SCENTED PLASTIC APPLICATOR TAMPONS receive FDA 510(k) clearance?

FEMTEX AND PRIVATE LABEL SCENTED PLASTIC APPLICATOR TAMPONS received FDA 510(k) clearance on 2003-09-03, under 510(k) number K032173.

Who is the listed applicant for FEMTEX AND PRIVATE LABEL SCENTED PLASTIC APPLICATOR TAMPONS?

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

What is the FDA product code for FEMTEX AND PRIVATE LABEL SCENTED PLASTIC APPLICATOR TAMPONS?

The FDA product code for FEMTEX AND PRIVATE LABEL SCENTED PLASTIC APPLICATOR TAMPONS 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 First Quality Hygienic, 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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