Device Classification Name |
system, imaging, pulsed doppler, ultrasonic
|
510(k) Number |
K051139 |
Device Name |
ACUSON SEQUOIA DIAGNOSTIC ULTRASOUND SYSTEM |
Applicant |
SIEMENS MEDICAL SOLUTIONS USA, INC. |
1230 SHOREBIRD WAY |
P O BOX 7393 |
MOUNTAIN VIEW,
CA
94039 -7393
|
|
Applicant Contact |
ISKRA MRAKOVIC |
Correspondent |
REGULATORY TECHNOLOGY SERVICES, LLC |
1000 Westgate Drive, |
Suite 510k |
Saint Paul,
MN
55114
|
|
Correspondent Contact |
MARK JOB |
Regulation Number | 892.1550
|
Classification Product Code |
|
Subsequent Product Codes |
|
Date Received | 05/04/2005 |
Decision Date | 05/13/2005 |
Decision |
Substantially Equivalent
(SESE) |
Regulation Medical Specialty |
Radiology
|
510k Review Panel |
Radiology
|
Summary |
Summary
|
Type |
Traditional
|
Reviewed by Third Party |
Yes
|
Combination Product |
No
|
|
|