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FDA 510(k)

PLAYTEX ULTIMATES UNSCENTED/SCENTED TAMPONS

K-Number: K914438 · 1992-01-02

Decision Date1992-01-02
Product CodeHIL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PLAYTEX ULTIMATES UNSCENTED/SCENTED TAMPONS is the device name listed in this FDA 510(k) record. The listed applicant is Playtex Family Products, Inc.. It received FDA 510(k) clearance on 1992-01-02 under 510(k) number K914438. 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 PLAYTEX ULTIMATES UNSCENTED/SCENTED TAMPONS?

PLAYTEX ULTIMATES UNSCENTED/SCENTED TAMPONS is a medical device that received FDA 510(k) clearance on 1992-01-02. The listed applicant is Playtex Family Products, Inc.. The 510(k) number is K914438.

When did PLAYTEX ULTIMATES UNSCENTED/SCENTED TAMPONS receive FDA 510(k) clearance?

PLAYTEX ULTIMATES UNSCENTED/SCENTED TAMPONS received FDA 510(k) clearance on 1992-01-02, under 510(k) number K914438.

Who is the listed applicant for PLAYTEX ULTIMATES UNSCENTED/SCENTED TAMPONS?

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

What is the FDA product code for PLAYTEX ULTIMATES UNSCENTED/SCENTED TAMPONS?

The FDA product code for PLAYTEX ULTIMATES UNSCENTED/SCENTED 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 Playtex Family Products, 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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