FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

3D/5D Viewer

K Number: K151808 · Decision Jul 29, 2015
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
15
Review Days
27

Basic Information

Device Name
3D/5D Viewer
K Number
K151808
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SAMSUNG MEDISON CO., LTD
Date Received
July 2, 2015
Decision Date
July 29, 2015
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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