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FDA 510(k)

LADY FREE UNSCENTED MENSTRUAL PAD

K-Number: K872287 · 1987-08-05

Decision Date1987-08-05
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

LADY FREE UNSCENTED MENSTRUAL PAD is the device name listed in this FDA 510(k) record. The listed applicant is American Tissue Corp.. It received FDA 510(k) clearance on 1987-08-05 under 510(k) number K872287. 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 LADY FREE UNSCENTED MENSTRUAL PAD?

LADY FREE UNSCENTED MENSTRUAL PAD is a medical device that received FDA 510(k) clearance on 1987-08-05. The listed applicant is American Tissue Corp.. The 510(k) number is K872287.

When did LADY FREE UNSCENTED MENSTRUAL PAD receive FDA 510(k) clearance?

LADY FREE UNSCENTED MENSTRUAL PAD received FDA 510(k) clearance on 1987-08-05, under 510(k) number K872287.

Who is the listed applicant for LADY FREE UNSCENTED MENSTRUAL PAD?

The FDA 510(k) record lists American Tissue Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LADY FREE UNSCENTED MENSTRUAL PAD?

The FDA product code for LADY FREE UNSCENTED MENSTRUAL PAD 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.

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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