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FDA 510(k)

PLAYTEX MODIFIED FIBER TAMPONS

K-Number: K811660 · 1981-07-16

ApplicantPlaytex, Inc.
Decision Date1981-07-16
Product CodeHIL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

PLAYTEX MODIFIED FIBER 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 1981-07-16 under 510(k) number K811660. 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 MODIFIED FIBER TAMPONS?

PLAYTEX MODIFIED FIBER TAMPONS is a medical device that received FDA 510(k) clearance on 1981-07-16. The listed applicant is Playtex, Inc.. The 510(k) number is K811660.

When did PLAYTEX MODIFIED FIBER TAMPONS receive FDA 510(k) clearance?

PLAYTEX MODIFIED FIBER TAMPONS received FDA 510(k) clearance on 1981-07-16, under 510(k) number K811660.

Who is the listed applicant for PLAYTEX MODIFIED FIBER 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 MODIFIED FIBER TAMPONS?

The FDA product code for PLAYTEX MODIFIED FIBER 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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