FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

Vitrea Software Package, VSTP-001A

K Number: K183013 · Decision Nov 26, 2018
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
87
Review Days
26

Basic Information

Device Name
Vitrea Software Package, VSTP-001A
K Number
K183013
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Canon Medical Systems Corporation
Date Received
October 31, 2018
Decision Date
November 26, 2018
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

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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