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

BARCODE CONICAL COLLIMATOR VERIFICATION (BCCV)

K Number: K103394 · Decision Jan 12, 2011
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
4
Review Days
54

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Basic Information

Device Name
BARCODE CONICAL COLLIMATOR VERIFICATION (BCCV)
K Number
K103394
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Varian Medical Systems, Oncology Systems
Date Received
November 19, 2010
Decision Date
January 12, 2011
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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Other Clearances by Varian Medical Systems, Oncology Systems

K Number Device Name
K123152 VITESSE 3.0
K101294 PT2 VARIAN PROTON THERAPY SYSTEM
K101751 VARIAN UNIQUE SINGLE ENERGY LINEAR ACCELERATOR