FDA 510(k)

DRIPRIDE DISPOSABLE UNDERPAD

K-Number: K881859 · 1988-06-03

Decision Date1988-06-03

Product CodeKME

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

DRIPRIDE DISPOSABLE UNDERPAD is the device name listed in this FDA 510(k) record. The listed applicant is Weyerhaeuser Co.. It received FDA 510(k) clearance on 1988-06-03 under 510(k) number K881859. The device is classified under product code KME. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRIPRIDE DISPOSABLE UNDERPAD?

DRIPRIDE DISPOSABLE UNDERPAD is a medical device that received FDA 510(k) clearance on 1988-06-03. The listed applicant is Weyerhaeuser Co.. The 510(k) number is K881859.

When did DRIPRIDE DISPOSABLE UNDERPAD receive FDA 510(k) clearance?

DRIPRIDE DISPOSABLE UNDERPAD received FDA 510(k) clearance on 1988-06-03, under 510(k) number K881859.

Who is the listed applicant for DRIPRIDE DISPOSABLE UNDERPAD?

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 DISPOSABLE UNDERPAD?

The FDA product code for DRIPRIDE DISPOSABLE UNDERPAD is KME.

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Other records listing Weyerhaeuser Co. as applicant

K883895DRIPRIDE ULTRA INCONTINENT PAD K883894DRIPRIDE PROVIDE SLIM K872059DRIPRIDE PROVIDE ULTRA K871725DRIPRIDE DISPOSABLE UNDERPADS K854408ADULT ABSORBENT INCONTINENT BRIEF K834359ABSORBENT INCONTINENT PADS & BRIEFS

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Related Devices (Code: KME)

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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.