FDA 510(k)

DRIPRIDE DISPOSABLE UNDERPADS

K-Number: K871725 · 1987-05-15

Decision Date1987-05-15

Product CodeKME

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

DRIPRIDE DISPOSABLE UNDERPADS is the device name listed in this FDA 510(k) record. The listed applicant is Weyerhaeuser Co.. It received FDA 510(k) clearance on 1987-05-15 under 510(k) number K871725. 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 UNDERPADS?

DRIPRIDE DISPOSABLE UNDERPADS is a medical device that received FDA 510(k) clearance on 1987-05-15. The listed applicant is Weyerhaeuser Co.. The 510(k) number is K871725.

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

DRIPRIDE DISPOSABLE UNDERPADS received FDA 510(k) clearance on 1987-05-15, under 510(k) number K871725.

Who is the listed applicant for DRIPRIDE DISPOSABLE UNDERPADS?

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 UNDERPADS?

The FDA product code for DRIPRIDE DISPOSABLE UNDERPADS is KME.

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Other records listing Weyerhaeuser Co. as applicant

K883895DRIPRIDE ULTRA INCONTINENT PAD K883894DRIPRIDE PROVIDE SLIM K881859DRIPRIDE DISPOSABLE UNDERPAD K872059DRIPRIDE PROVIDE ULTRA 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.