DUAL LUMEN MIDLINE CATHETER


Device Classification Name

catheter,intravascular,therapeutic,long-term greater than 30 days

510(k) Number K010349
Device Name DUAL LUMEN MIDLINE CATHETER
Original Applicant
CATHETER INNOVATIONS, INC.
3598 west 1820 south
salt lake city, 
UT 
84104

Original Contact roger l richins
Regulation Number 880.5970
Classification Product Code
LJS  
Date Received 02/05/2001
Decision Date 02/28/2001
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General Hospital

510k Review Panel

General Hospital

Type Special
Reviewed by Third Party No

Combination Product

No

Category: Uncategorized