FDA 510(k) FDA class 2 Substantially Equivalent 🇧🇪 Belgium

Proton Immobilization Solution

K Number: K151207 · Decision Jul 28, 2015
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
9
Review Days
83

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Basic Information

Device Name
Proton Immobilization Solution
K Number
K151207
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Orfit Industries NV
Date Received
May 6, 2015
Decision Date
July 28, 2015
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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