VAS-CATH DUALATOR(TM) VESSEL DILATOR— 510(k) K914210

Name: FDA 510(k) clearance K914210
Creator: U.S. Food and Drug Administration
Published: 1993-07-01

Substantially Equivalent

Vas-Cath, Inc.

FDA 510(k) clearance K914210 for VAS-CATH DUALATOR(TM) VESSEL DILATOR, Substantially Equivalent on 1993-07-01. Applicant: Vas-Cath, Inc.. Device class: 2.

Clearance details

Applicant: Vas-Cath, Inc.
Product code: Code FKA
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1991-09-19
Decision date: 1993-07-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mississauga, Ontario, CA

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