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FDA 510(k)

ALWAYS MENSTRUAL PADS

K-Number: K071827 · 2007-09-20

Decision Date2007-09-20
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ALWAYS MENSTRUAL PADS is the device name listed in this FDA 510(k) record. The listed applicant is Procter & Gamble, Inc.. It received FDA 510(k) clearance on 2007-09-20 under 510(k) number K071827. 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 ALWAYS MENSTRUAL PADS?

ALWAYS MENSTRUAL PADS is a medical device that received FDA 510(k) clearance on 2007-09-20. The listed applicant is Procter & Gamble, Inc.. The 510(k) number is K071827.

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

ALWAYS MENSTRUAL PADS received FDA 510(k) clearance on 2007-09-20, under 510(k) number K071827.

Who is the listed applicant for ALWAYS MENSTRUAL PADS?

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

What is the FDA product code for ALWAYS MENSTRUAL PADS?

The FDA product code for ALWAYS 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.

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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