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FDA 510(k)

SCENTED MENSTRUAL PADS

K-Number: K812403 · 1981-09-09

Decision Date1981-09-09
Product CodeHHL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SCENTED MENSTRUAL PADS is the device name listed in this FDA 510(k) record. The listed applicant is Procter & Gamble Mfg. Co.. It received FDA 510(k) clearance on 1981-09-09 under 510(k) number K812403. The device is classified under product code HHL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCENTED MENSTRUAL PADS?

SCENTED MENSTRUAL PADS is a medical device that received FDA 510(k) clearance on 1981-09-09. The listed applicant is Procter & Gamble Mfg. Co.. The 510(k) number is K812403.

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

SCENTED MENSTRUAL PADS received FDA 510(k) clearance on 1981-09-09, under 510(k) number K812403.

Who is the listed applicant for SCENTED MENSTRUAL PADS?

The FDA 510(k) record lists Procter & Gamble Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCENTED MENSTRUAL PADS?

The FDA product code for SCENTED MENSTRUAL PADS is HHL.

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 Procter & Gamble Mfg. 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 72 devices →

Related Devices (Code: HHL)

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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