CONTINUOUS ARTERIAL/VENOUS HEMOFILTRATION TRAY— 510(k) K880775

Name: FDA 510(k) clearance K880775
Creator: U.S. Food and Drug Administration
Published: 1988-07-25

Unknown

Medsurg Industries, Inc.

FDA 510(k) clearance K880775 for CONTINUOUS ARTERIAL/VENOUS HEMOFILTRATION TRAY, Unknown on 1988-07-25. Applicant: Medsurg Industries, Inc.. Device class: 2.

Clearance details

Applicant: Medsurg Industries, Inc.
Product code: Code LFK
Device class: Class 2
Regulation: 21 CFR 876.5540
Advisory panel: Gastroenterology, Urology
Date received: 1988-02-26
Decision date: 1988-07-25
Decision: Unknown
Clearance type: Traditional
Location: Herndon, VA, US

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