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FDA 510(k)

UNSCENTED MENSTRUAL PADS

K-Number: K880735 · 1988-04-25

Decision Date1988-04-25
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

UNSCENTED MENSTRUAL PADS 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 1988-04-25 under 510(k) number K880735. 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 UNSCENTED MENSTRUAL PADS?

UNSCENTED MENSTRUAL PADS is a medical device that received FDA 510(k) clearance on 1988-04-25. The listed applicant is Personal Products Co.. The 510(k) number is K880735.

When did UNSCENTED MENSTRUAL PADS receive FDA 510(k) clearance?

UNSCENTED MENSTRUAL PADS received FDA 510(k) clearance on 1988-04-25, under 510(k) number K880735.

Who is the listed applicant for UNSCENTED MENSTRUAL PADS?

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 UNSCENTED MENSTRUAL PADS?

The FDA product code for UNSCENTED MENSTRUAL PADS 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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