Cordis Endeavor Infusion Catheter— 510(k) K972110

Substantially Equivalent

Cordis Corp.

FDA 510(k) clearance K972110 for Cordis Endeavor Infusion Catheter, Substantially Equivalent on 1997-08-14. Applicant: Cordis Corp..

Clearance details

Applicant: Cordis Corp.
Product code: Code QEY
Advisory panel: Cardiovascular
Date received: 1997-06-05
Decision date: 1997-08-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami Lakes, FL, US

Download summary PDF View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.