CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH. KITS— 510(k) K915215

Name: FDA 510(k) clearance K915215
Creator: U.S. Food and Drug Administration
Published: 1992-03-27

Unknown

Akcess Medical Products, Inc.

FDA 510(k) clearance K915215 for CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH. KITS, Unknown on 1992-03-27. Applicant: Akcess Medical Products, Inc.. Device class: 2.

Clearance details

Applicant: Akcess Medical Products, Inc.
Product code: Code LFK
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1991-11-18
Decision date: 1992-03-27
Decision: Unknown
Clearance type: Traditional
Location: New Brunswick, NJ, US

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