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

PROFILER 2

K Number: K063021 · Decision Nov 22, 2006
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
13
Review Days
51

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Basic Information

Device Name
PROFILER 2
K Number
K063021
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sun Nuclear Corp.
Date Received
October 2, 2006
Decision Date
November 22, 2006
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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K Number Device Name
K112981 SUN 125C IONIZATION CHAMBER
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K092019 MODEL 1014 PC ELECTROMETER
K051921 THE EDGE DETECTOR, MODEL 1118
K013689 RE-ENTRANT CHAMBER
K021463 MODEL 1133 IVD PC VERSION
K011332 RF-IVD WIRELESS DOSIMETER-MODEL 1133
K011466 QED DIODE DETECTORS, MODELS 1112-1116
K010449 IVD (IN VIVO DOSIMETER), MODEL 1131
K002446 RE-ENTRANT CHAMBER, MODEL 1008 OR 44D
Search all 13 clearances from Sun Nuclear Corp. →