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FDA 510(k)

ADULT INCONTINET BRIEF

K-Number: K821397 · 1982-05-24

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1982-05-24
Product CodeEYQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ADULT INCONTINET BRIEF is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1982-05-24 under 510(k) number K821397. 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 ADULT INCONTINET BRIEF?

ADULT INCONTINET BRIEF is a medical device that received FDA 510(k) clearance on 1982-05-24. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K821397.

When did ADULT INCONTINET BRIEF receive FDA 510(k) clearance?

ADULT INCONTINET BRIEF received FDA 510(k) clearance on 1982-05-24, under 510(k) number K821397.

Who is the listed applicant for ADULT INCONTINET BRIEF?

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

What is the FDA product code for ADULT INCONTINET BRIEF?

The FDA product code for ADULT INCONTINET BRIEF is EYQ.

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Related Devices (Code: EYQ)

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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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