CORDIS INTRODUCER GUIDE


codes

Device Classification Name

catheter, percutaneous

510(k) Number K001136
Device Name CORDIS INTRODUCER GUIDE
Original Applicant
CORDIS CORP.
14201 n.w. 60th ave.
miami lakes, 
FL 
33014

Original Contact ariel mactavish
Regulation Number 870.1250
Classification Product Code
DQY  
Date Received 04/10/2000
Decision Date 04/28/2000
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Cardiovascular

510k Review Panel

Cardiovascular

Type Special
Reviewed by Third Party No

Combination Product

No