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FDA 510(k)

ALWAYS CONTOURS UNSCENTED MENSTRUAL PADS

K-Number: K922575 · 1993-02-02

Decision Date1993-02-02
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ALWAYS CONTOURS UNSCENTED MENSTRUAL PADS 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 1993-02-02 under 510(k) number K922575. 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 CONTOURS UNSCENTED MENSTRUAL PADS?

ALWAYS CONTOURS UNSCENTED MENSTRUAL PADS is a medical device that received FDA 510(k) clearance on 1993-02-02. The listed applicant is Procter & Gamble Co.. The 510(k) number is K922575.

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

ALWAYS CONTOURS UNSCENTED MENSTRUAL PADS received FDA 510(k) clearance on 1993-02-02, under 510(k) number K922575.

Who is the listed applicant for ALWAYS CONTOURS UNSCENTED MENSTRUAL PADS?

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 CONTOURS UNSCENTED MENSTRUAL PADS?

The FDA product code for ALWAYS CONTOURS 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 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: 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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