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

PROBEAM PROTON THERAPY SYSTEM

K Number: K133191 · Decision Jan 10, 2014
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
91
Applicant Total
33
Review Days
85

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Basic Information

Device Name
PROBEAM PROTON THERAPY SYSTEM
K Number
K133191
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
Date Received
October 17, 2013
Decision Date
January 10, 2014
Product Code
LHN
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
LHN System, Radiation Therapy, Charged-Particle, Medical

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Other Clearances by Varian Medical Systems

K Number Device Name
K252717 MAASTRO Rectal Applicator Set
K252884 Guided Aarhus Applicator Set
K250099 Mobius3D (4.1)
K250289 Intracavitary/Interstitial System
K242378 Eclipse Treatment Planning System (18.1)
K242961 Intraluminal Applicator Set
K241965 Catheter Surface Flap Applicator Set (GM11011830)
K241876 Vitesse (5.0)
K232400 VariSeed (v10)
K124002 VERIFICATION CONSOLE
Search all 33 clearances from Varian Medical Systems →