V.F.I.-VISCOUS FLUID INFUSION TUBING SET— 510(k) K981907

Name: FDA 510(k) clearance K981907
Creator: U.S. Food and Drug Administration
Published: 1998-08-04

Substantially Equivalent

Peregrine Surgical , Ltd.

FDA 510(k) clearance K981907 for V.F.I.-VISCOUS FLUID INFUSION TUBING SET, Substantially Equivalent on 1998-08-04. Applicant: Peregrine Surgical , Ltd.. Device class: 2.

Clearance details

Applicant: Peregrine Surgical , Ltd.
Product code: Code MRH
Device class: Class 2
Regulation: 21 CFR 880.5725
Advisory panel: General Hospital
Date received: 1998-06-01
Decision date: 1998-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Doylestown, PA, US

Download summary PDF View on FDA.gov ↗

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