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

CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEM

K Number: K992753 · Decision Sep 3, 1999
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
255
Applicant Total
86
Review Days
18

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Basic Information

Device Name
CADPLAN PLUS: 3D TREATMENT PLANNING SYSTEM
K Number
K992753
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Varian Assoc., Inc.
Date Received
August 16, 1999
Decision Date
September 3, 1999
Product Code
MUJ
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
MUJ System, Planning, Radiation Therapy Treatment

Similar 510(k) Clearances

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Other Clearances by Varian Assoc., Inc.

K Number Device Name
K000922 PROTON VISION
K992762 BRACHYVISION 6.0
K992751 SOMAVISION
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
K943224 VARIAN MULTILEAF COLLIMATOR
K952913 APPLICATORS FOR VARIAN VARISOURCE REMOTE HIGH SOES RATE AFTERLOADER
Search all 86 clearances from Varian Assoc., Inc. →