LABELING CHANGE - VIASPAN(TM) (BELZER UW)— 510(k) K900492

Name: FDA 510(k) clearance K900492
Creator: U.S. Food and Drug Administration
Published: 1990-03-20

Substantially Equivalent

The DU Pont Co.

FDA 510(k) clearance K900492 for LABELING CHANGE - VIASPAN(TM) (BELZER UW), Substantially Equivalent on 1990-03-20. Applicant: The DU Pont Co.. Device class: 2.

Clearance details

Applicant: The DU Pont Co.
Product code: Code KDL
Device class: Class 2
Regulation: 21 CFR 876.5880
Advisory panel: Gastroenterology, Urology
Date received: 1990-02-02
Decision date: 1990-03-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wilmington, DE, US

Download summary PDF View on FDA.gov ↗

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