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FDA 510(k)

ALWAYS DUETS

K-Number: K012629 · 2001-10-05

ApplicantProcter & Gamble Co.
Decision Date2001-10-05
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ALWAYS DUETS 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 2001-10-05 under 510(k) number K012629. 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 DUETS?

ALWAYS DUETS is a medical device that received FDA 510(k) clearance on 2001-10-05. The listed applicant is Procter & Gamble Co.. The 510(k) number is K012629.

When did ALWAYS DUETS receive FDA 510(k) clearance?

ALWAYS DUETS received FDA 510(k) clearance on 2001-10-05, under 510(k) number K012629.

Who is the listed applicant for ALWAYS DUETS?

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 DUETS?

The FDA product code for ALWAYS DUETS is HHD.

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Other records listing Procter & Gamble Co. as applicant

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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.

K071827ALWAYS MENSTRUAL PADSProcter & Gamble, Inc.K003843ENVIVE MINIFORMSProcter & Gamble Co.K993870UNSCENTED INTERLABIAL MENSTRUAL PADProcter & Gamble Co.K980395GLADRAGS COTTON MENSTRUAL PADKeepers!, Inc.K953470FLUSHIES FLUSHABLE/BIODEGRADABLE MENSTRUAL PADS/NAPKINS (ULTRA THINS)Mediquip, Inc.K953667UNSCENTED CURVED ULTRATHIN MAXI PADSParagon Trade Brands, Inc.

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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