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

Nucleus Image Management System

K Number: K171130 · Decision May 4, 2017
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
2
Review Days
17

Basic Information

Device Name
Nucleus Image Management System
K Number
K171130
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
NucleusHealth, LLC
Date Received
April 17, 2017
Decision Date
May 4, 2017
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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Other Clearances by NucleusHealth, LLC

K Number Device Name
K203249 Nucleus.io