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

VARIAN MULTILEAF COLLIMATOR

K Number: K943224 · Decision Feb 2, 1996
Classifications
1
FEI Numbers
123
Registration Numbers
124
Same Product Code
717
Applicant Total
86
Review Days
577

Basic Information

Device Name
VARIAN MULTILEAF COLLIMATOR
K Number
K943224
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
VARIAN ASSOC., INC.
Date Received
July 5, 1994
Decision Date
February 2, 1996
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 ASSOC., INC.

K Number Device Name
K000922 PROTON VISION
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K992751 SOMAVISION
K992753 CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEM
K990085 MILLENNIUM MLC -120
K980601 VARISOURCE WRIGHT VAGINAL CUFF APPLICATOR FOR VARIAN VARISOURCE REMOTE HIGH DOSE RATE AFTERIOADER
K955844 APPLICATORS FOR VARIAN VARISOURCE REMOTE HIGH DOSE RATE AFTERLOADER
K955774 VARIS PORTALVISION
K954467 CADPLAN BT
K952913 APPLICATORS FOR VARIAN VARISOURCE REMOTE HIGH SOES RATE AFTERLOADER
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