FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

CLARITY

K Number: K121663 · Decision Dec 5, 2012
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
10
Review Days
183

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Basic Information

Device Name
CLARITY
K Number
K121663
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Elekta , Ltd.
Date Received
June 5, 2012
Decision Date
December 5, 2012
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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