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FDA 510(k) Application Details - K070322
Device Classification Name
System, Image Processing, Radiological
More FDA Info for this Device
510(K) Number
K070322
Device Name
System, Image Processing, Radiological
Applicant
SIEMENS MEDICAL SOLUTIONS USA, INC.
400 W. MORGAN ROAD
SUITE 100
ANN ARBOR, MI 48108-9117 US
Other 510(k) Applications for this Company
Contact
SIEGLINDE NINA WEST
Other 510(k) Applications for this Contact
Regulation Number
892.2050
More FDA Info for this Regulation Number
Classification Product Code
LLZ
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
02/02/2007
Decision Date
02/27/2007
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
Y
Expedited Review
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