CORPATH 200 SYSTEM— 510(k) K120834

Substantially Equivalent

Corindus, Inc.

FDA 510(k) clearance K120834 for CORPATH 200 SYSTEM, Substantially Equivalent on 2012-07-19. Applicant: Corindus, Inc..

Clearance details

Applicant: Corindus, Inc.
Product code: Code DXX
Advisory panel: Cardiovascular
Date received: 2012-03-19
Decision date: 2012-07-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Baltimore, MD, US

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