DRIPRIDE ULTRA INCONTINENT PAD— 510(k) K883895

Name: FDA 510(k) clearance K883895
Creator: U.S. Food and Drug Administration
Published: 1989-01-30

Substantially Equivalent

Weyerhaeuser Co.

FDA 510(k) clearance K883895 for DRIPRIDE ULTRA INCONTINENT PAD, Substantially Equivalent on 1989-01-30. Applicant: Weyerhaeuser Co.. Device class: 1.

Clearance details

Applicant: Weyerhaeuser Co.
Product code: Code EYQ
Device class: Class 1
Regulation: 21 CFR 876.5920
Advisory panel: Gastroenterology, Urology
Date received: 1988-09-14
Decision date: 1989-01-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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More clearances from Weyerhaeuser Co.

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K883894 — DRIPRIDE PROVIDE SLIM1989-01-30
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K872059 — DRIPRIDE PROVIDE ULTRA1988-03-16
K871725 — DRIPRIDE DISPOSABLE UNDERPADS1987-05-15
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