Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ALWAYS, UNSCENTED MENSTRUAL PAD

K-Number: K913238 · 1991-09-23

Decision Date1991-09-23
Product CodeHHL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ALWAYS, UNSCENTED MENSTRUAL PAD is the device name listed in this FDA 510(k) record. The listed applicant is Procter & Gamble Co.. It received FDA 510(k) clearance on 1991-09-23 under 510(k) number K913238. 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 ALWAYS, UNSCENTED MENSTRUAL PAD?

ALWAYS, UNSCENTED MENSTRUAL PAD is a medical device that received FDA 510(k) clearance on 1991-09-23. The listed applicant is Procter & Gamble Co.. The 510(k) number is K913238.

When did ALWAYS, UNSCENTED MENSTRUAL PAD receive FDA 510(k) clearance?

ALWAYS, UNSCENTED MENSTRUAL PAD received FDA 510(k) clearance on 1991-09-23, under 510(k) number K913238.

Who is the listed applicant for ALWAYS, UNSCENTED MENSTRUAL PAD?

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

What is the FDA product code for ALWAYS, UNSCENTED MENSTRUAL PAD?

The FDA product code for ALWAYS, UNSCENTED MENSTRUAL PAD 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 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 22 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

View on FDA Database →

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

↑