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FDA 510(k) Application Details - K150843
Device Classification Name
System, Image Processing, Radiological
More FDA Info for this Device
510(K) Number
K150843
Device Name
System, Image Processing, Radiological
Applicant
Siemens AG
Henkestrasse 127
Eriangen 91052 DE
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Contact
Martin Meyer
Other 510(k) Applications for this Contact
Regulation Number
892.2050
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Classification Product Code
LLZ
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More FDA Info for this Product Code
Date Received
03/30/2015
Decision Date
04/24/2015
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
RA - Radiology
Review Advisory Committee
RA - Radiology
Statement / Summary / Purged Status
Summary
Type
Abbreviated
Reviewed By Third Party
Y
Expedited Review
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