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

Accuray Precision Treatment Planning System

K Number: K212794 · Decision Sep 30, 2021
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
21
Review Days
28

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Basic Information

Device Name
Accuray Precision Treatment Planning System
K Number
K212794
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Accuray Incorporated
Date Received
September 2, 2021
Decision Date
September 30, 2021
Product Code
IYE
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
IYE Accelerator, Linear, Medical

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