CYPRESS ULTRASOUND SYSTEM


Device Classification Name

system, imaging, pulsed doppler, ultrasonic

510(k) Number K021497
Device Name CYPRESS ULTRASOUND SYSTEM
Original Applicant
ACUSON CORP.
1220 charleston rd.
mountain view, 
CA 
94039 -7393

Original Contact bob leiker
Regulation Number 892.1550
Classification Product Code
IYN  
Subsequent Product Codes
ITX   IYO  
Date Received 05/09/2002
Decision Date 07/09/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Radiology

510k Review Panel

Radiology

summary

summary

Type Special
Reviewed by Third Party No

Combination Product

No

Recalls CDRH Recalls