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

Precision Treatment Planning System

K Number: K161136 · Decision Jun 24, 2016
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
255
Applicant Total
21
Review Days
63

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Basic Information

Device Name
Precision Treatment Planning System
K Number
K161136
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Accuray Incorporated
Date Received
April 22, 2016
Decision Date
June 24, 2016
Product Code
MUJ
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
MUJ System, Planning, Radiation Therapy Treatment

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K Number Device Name
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K182687 Motion Tracking and Compensation Feature for the Radixact Treatment Delivery System
K171837 TomoTherapy Treatment Delivery System with iDMS
K171086 Accuray Precision Treatment Planning System
K161146 Radixact Treatment Delivery System
K161144 iDMS Data Management System
K152488 Onrad Treatment System
K150873 CyberKnife M6 FI Sytem, CyberKnife M6 FM System, CyberKnife M6 FIM System
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