MODEL 600 VASCULAR DUPLEX IMAGER— 510(k) K863589

Name: FDA 510(k) clearance K863589
Creator: U.S. Food and Drug Administration
Published: 1987-06-24

Substantially Equivalent

Multigon Industries, Inc.

FDA 510(k) clearance K863589 for MODEL 600 VASCULAR DUPLEX IMAGER, Substantially Equivalent on 1987-06-24. Applicant: Multigon Industries, Inc.. Device class: 2.

Clearance details

Applicant: Multigon Industries, Inc.
Product code: Code DXK
Device class: Class 2
Regulation: 21 CFR 870.2330
Advisory panel: Cardiovascular
Date received: 1986-09-15
Decision date: 1987-06-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mt. Vernon, NY, US

Download summary PDF View on FDA.gov ↗

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