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FDA 510(k)

PLAYTEX SLENDER REGULAR TAMPONS

K-Number: K841154 · 1984-03-19

ApplicantPlaytex, Inc.
Decision Date1984-03-19
Product CodeHIL
Advisory CommitteeOB
DecisionUnknown

Device Summary

PLAYTEX SLENDER REGULAR TAMPONS is the device name listed in this FDA 510(k) record. The listed applicant is Playtex, Inc.. It received FDA 510(k) clearance on 1984-03-19 under 510(k) number K841154. The device is classified under product code HIL. It was reviewed by the OB advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the PLAYTEX SLENDER REGULAR TAMPONS?

PLAYTEX SLENDER REGULAR TAMPONS is a medical device that received FDA 510(k) clearance on 1984-03-19. The listed applicant is Playtex, Inc.. The 510(k) number is K841154.

When did PLAYTEX SLENDER REGULAR TAMPONS receive FDA 510(k) clearance?

PLAYTEX SLENDER REGULAR TAMPONS received FDA 510(k) clearance on 1984-03-19, under 510(k) number K841154.

Who is the listed applicant for PLAYTEX SLENDER REGULAR TAMPONS?

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

What is the FDA product code for PLAYTEX SLENDER REGULAR TAMPONS?

The FDA product code for PLAYTEX SLENDER REGULAR 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, 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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