FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

vRad PACS with Mammography

K Number: K162145 · Decision Oct 25, 2016
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
2
Review Days
85

Basic Information

Device Name
vRad PACS with Mammography
K Number
K162145
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Virtual Radiologic Corporation
Date Received
August 1, 2016
Decision Date
October 25, 2016
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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K Number Device Name
K241879 vRad Viewer