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

Delivery Analysis

K Number: K143269 · Decision Apr 14, 2015
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
255
Applicant Total
21
Review Days
152

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Basic Information

Device Name
Delivery Analysis
K Number
K143269
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
November 13, 2014
Decision Date
April 14, 2015
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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Other Clearances by Accuray Incorporated

K Number Device Name
K223159 Radixact Treatment Delivery System
K212794 Accuray Precision Treatment Planning System
K202412 ClearRT Helical kVCT for the Radixact Treatment Delivery System
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
K161136 Precision Treatment Planning System
K161144 iDMS Data Management System
K152488 Onrad Treatment System
Search all 21 clearances from Accuray Incorporated →