CYPRESS SYSTEM


Device Classification Name

system, imaging, pulsed echo, ultrasonic

510(k) Number K010950
Device Name CYPRESS SYSTEM
Original Applicant
ACUSON CORP.
555 13th st., n.w.
washington, 
DC 
20004 -1109

Original Contact howard m holstein
Regulation Number 892.1560
Classification Product Code
IYO  
Date Received 03/29/2001
Decision Date 06/27/2001
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Radiology

510k Review Panel

Radiology

Type Abbreviated
Reviewed by Third Party No

Combination Product

No