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FDA 510(k)

PLAYTEX FLUSHABLE TAMPONS, REGULAR, SUPER, SUPER +

K-Number: K924279 · 1993-05-21

Decision Date1993-05-21
Product CodeHIL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PLAYTEX FLUSHABLE TAMPONS, REGULAR, SUPER, SUPER + 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 1993-05-21 under 510(k) number K924279. 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 FLUSHABLE TAMPONS, REGULAR, SUPER, SUPER +?

PLAYTEX FLUSHABLE TAMPONS, REGULAR, SUPER, SUPER + is a medical device that received FDA 510(k) clearance on 1993-05-21. The listed applicant is Playtex Family Products, Inc.. The 510(k) number is K924279.

When did PLAYTEX FLUSHABLE TAMPONS, REGULAR, SUPER, SUPER + receive FDA 510(k) clearance?

PLAYTEX FLUSHABLE TAMPONS, REGULAR, SUPER, SUPER + received FDA 510(k) clearance on 1993-05-21, under 510(k) number K924279.

Who is the listed applicant for PLAYTEX FLUSHABLE TAMPONS, REGULAR, SUPER, SUPER +?

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 FLUSHABLE TAMPONS, REGULAR, SUPER, SUPER +?

The FDA product code for PLAYTEX FLUSHABLE TAMPONS, REGULAR, SUPER, SUPER + 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.

View all 17 devices →

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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