CINESCAN S


Device Classification Name

system, imaging, pulsed echo, ultrasonic

510(k) Number K021683
Device Name CINESCAN S
Original Applicant
QUANTEL MEDICAL
377 route 17 south
hasbrouck heights, 
NJ 
07604

Original Contact george myers
Regulation Number 892.1560
Classification Product Code
IYO  
Date Received 05/22/2002
Decision Date 06/21/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Radiology

510k Review Panel

Radiology

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No