FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

SYNGO.VIA

K Number: K123375 · Decision Nov 20, 2012
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
15
Review Days
19

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Basic Information

Device Name
SYNGO.VIA
K Number
K123375
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Siemens AG
Date Received
November 1, 2012
Decision Date
November 20, 2012
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LLZ System, Image Processing, Radiological

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