VASCULAR ARCHITECTS PERISCOPE DEVICE— 510(k) K003719

Substantially Equivalent

Vascular Architects, Inc.

FDA 510(k) clearance K003719 for VASCULAR ARCHITECTS PERISCOPE DEVICE, Substantially Equivalent on 2001-02-28. Applicant: Vascular Architects, Inc..

Clearance details

Applicant: Vascular Architects, Inc.
Product code: Code DWX
Advisory panel: Cardiovascular
Date received: 2000-12-04
Decision date: 2001-02-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Jose, CA, US

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