FDA 510(k)

ADULT ABSORBENT INCONTINENT BRIEF

K-Number: K854408 · 1985-11-19

Decision Date1985-11-19

Product CodeEYQ

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

ADULT ABSORBENT INCONTINENT BRIEF is the device name listed in this FDA 510(k) record. The listed applicant is Weyerhaeuser Co.. It received FDA 510(k) clearance on 1985-11-19 under 510(k) number K854408. 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 ABSORBENT INCONTINENT BRIEF?

ADULT ABSORBENT INCONTINENT BRIEF is a medical device that received FDA 510(k) clearance on 1985-11-19. The listed applicant is Weyerhaeuser Co.. The 510(k) number is K854408.

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

ADULT ABSORBENT INCONTINENT BRIEF received FDA 510(k) clearance on 1985-11-19, under 510(k) number K854408.

Who is the listed applicant for ADULT ABSORBENT INCONTINENT BRIEF?

The FDA 510(k) record lists Weyerhaeuser Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ADULT ABSORBENT INCONTINENT BRIEF?

The FDA product code for ADULT ABSORBENT INCONTINENT BRIEF is EYQ.

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Other records listing Weyerhaeuser Co. as applicant

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Related Devices (Code: EYQ)

K950784DRISTAR URINARY INCONTINENCE MANAGEMENT SYSTEMAdvanced Bioresearch Assoc.K932310KIT PAK INCONTINENT SKIN CARE KITKit Pak, Inc.K903342DEODORIZING AND SOUND MUFFLING ANAL PADBiological Resistance, Inc.K891686LIB SYSTEM, BABY/ADULT DIAPERIntera Corp.K885185INTERA SHIELD AND INTERA UNDERGARMENTIntera Corp.K883894DRIPRIDE PROVIDE SLIMWeyerhaeuser Co.

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.