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FDA 510(k)

DRIPRIDE ULTRA INCONTINENT PAD

K-Number: K883895 · 1989-01-30

ApplicantWeyerhaeuser Co.
Decision Date1989-01-30
Product CodeEYQ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DRIPRIDE ULTRA INCONTINENT PAD is the device name listed in this FDA 510(k) record. The listed applicant is Weyerhaeuser Co.. It received FDA 510(k) clearance on 1989-01-30 under 510(k) number K883895. 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 DRIPRIDE ULTRA INCONTINENT PAD?

DRIPRIDE ULTRA INCONTINENT PAD is a medical device that received FDA 510(k) clearance on 1989-01-30. The listed applicant is Weyerhaeuser Co.. The 510(k) number is K883895.

When did DRIPRIDE ULTRA INCONTINENT PAD receive FDA 510(k) clearance?

DRIPRIDE ULTRA INCONTINENT PAD received FDA 510(k) clearance on 1989-01-30, under 510(k) number K883895.

Who is the listed applicant for DRIPRIDE ULTRA INCONTINENT PAD?

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 DRIPRIDE ULTRA INCONTINENT PAD?

The FDA product code for DRIPRIDE ULTRA INCONTINENT PAD 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.

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Other records listing Weyerhaeuser 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.

K883894DRIPRIDE PROVIDE SLIMK881859DRIPRIDE DISPOSABLE UNDERPADK872059DRIPRIDE PROVIDE ULTRAK871725DRIPRIDE DISPOSABLE UNDERPADSK854408ADULT ABSORBENT INCONTINENT BRIEFK834359ABSORBENT INCONTINENT PADS & BRIEFS

View all 10 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.

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.

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