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FDA 510(k)

ATTENDS INCONTINENT UNDERGARMENT

K-Number: K850611 · 1985-02-26

Decision Date1985-02-26
Product CodeEYQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ATTENDS INCONTINENT UNDERGARMENT 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 1985-02-26 under 510(k) number K850611. The device is classified under product code EYQ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATTENDS INCONTINENT UNDERGARMENT?

ATTENDS INCONTINENT UNDERGARMENT is a medical device that received FDA 510(k) clearance on 1985-02-26. The listed applicant is Procter & Gamble Mfg. Co.. The 510(k) number is K850611.

When did ATTENDS INCONTINENT UNDERGARMENT receive FDA 510(k) clearance?

ATTENDS INCONTINENT UNDERGARMENT received FDA 510(k) clearance on 1985-02-26, under 510(k) number K850611.

Who is the listed applicant for ATTENDS INCONTINENT UNDERGARMENT?

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 ATTENDS INCONTINENT UNDERGARMENT?

The FDA product code for ATTENDS INCONTINENT UNDERGARMENT is EYQ.

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: EYQ)

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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