Cordis Endeavor Infusion Catheter— 510(k) K970842

Substantially Equivalent

Cordis Corp.

FDA 510(k) clearance K970842 for Cordis Endeavor Infusion Catheter, Substantially Equivalent on 1997-05-28. Applicant: Cordis Corp..

Clearance details

Applicant: Cordis Corp.
Product code: Code QEY
Advisory panel: Cardiovascular
Date received: 1997-03-07
Decision date: 1997-05-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami Lakes, FL, US

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