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FDA 510(k)

MODESS* BELTLESS FEMININE NAPKIN

K-Number: K781470 · 1978-09-07

Decision Date1978-09-07
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MODESS* BELTLESS FEMININE NAPKIN is the device name listed in this FDA 510(k) record. The listed applicant is Personal Products Co.. It received FDA 510(k) clearance on 1978-09-07 under 510(k) number K781470. The device is classified under product code HHD. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODESS* BELTLESS FEMININE NAPKIN?

MODESS* BELTLESS FEMININE NAPKIN is a medical device that received FDA 510(k) clearance on 1978-09-07. The listed applicant is Personal Products Co.. The 510(k) number is K781470.

When did MODESS* BELTLESS FEMININE NAPKIN receive FDA 510(k) clearance?

MODESS* BELTLESS FEMININE NAPKIN received FDA 510(k) clearance on 1978-09-07, under 510(k) number K781470.

Who is the listed applicant for MODESS* BELTLESS FEMININE NAPKIN?

The FDA 510(k) record lists Personal Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODESS* BELTLESS FEMININE NAPKIN?

The FDA product code for MODESS* BELTLESS FEMININE NAPKIN is HHD.

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 Personal Products Co. 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 45 devices →

Related Devices (Code: HHD)

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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