MODIFICATION TO TISSUELINK MONOPOLAR FLOATING BALL


Device Classification Name

electrosurgical, cutting & coagulation & accessories

510(k) Number K010662
Device Name MODIFICATION TO TISSUELINK MONOPOLAR FLOATING BALL
Original Applicant
TISSUELINK MEDICAL, INC.
one washington center
suite 400
dover, 
NH 

Original Contact roberta thompson
Regulation Number 878.4400
Classification Product Code
GEI  
Date Received 03/01/2001
Decision Date 04/27/2001
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

General & Plastic Surgery

510k Review Panel

General & Plastic Surgery

Type Traditional
Reviewed by Third Party No

Combination Product

No