CORDIS 13F CATHETER SHEATH INTRODUCER


information about

Device Classification Name

catheter, electrode recording, or probe, electrode recording

510(k) Number K000753
Device Name CORDIS 13F CATHETER SHEATH INTRODUCER
Original Applicant
CORDIS CORP.
14201 n.w. 60th ave.
miami lakes, 
FL 
33014

Original Contact ariel mactavish
Regulation Number 870.1220
Classification Product Code
DRF  
Date Received 03/08/2000
Decision Date 04/06/2000
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

Type Special
Reviewed by Third Party No

Combination Product

No