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

syngo.plaza

K Number: K180563 · Decision Apr 25, 2018
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
19
Review Days
51

Basic Information

Device Name
syngo.plaza
K Number
K180563
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Siemens Healthcare GmbH
Date Received
March 5, 2018
Decision Date
April 25, 2018
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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