MODIFICATION HEMOFILTRATION CATHETER HF-100— 510(k) K890717

Substantially Equivalent

Vas-Cath, Inc.

FDA 510(k) clearance K890717 for MODIFICATION HEMOFILTRATION CATHETER HF-100, Substantially Equivalent on 1989-04-05. Applicant: Vas-Cath, Inc..

Clearance details

Applicant: Vas-Cath, Inc.
Product code: Code LFK
Advisory panel: Gastroenterology, Urology
Date received: 1989-02-13
Decision date: 1989-04-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mississauga, Ontario, CA

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