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

VARIAN INTRACAVITARY BRACHYTHERAPY APPLICATORS

K Number: K033371 · Decision Dec 24, 2003
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
206
Applicant Total
33
Review Days
64

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Basic Information

Device Name
VARIAN INTRACAVITARY BRACHYTHERAPY APPLICATORS
K Number
K033371
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5700
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Varian Medical Systems
Date Received
October 21, 2003
Decision Date
December 24, 2003
Product Code
JAQ
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
JAQ System, Applicator, Radionuclide, Remote-Controlled

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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)
K133191 PROBEAM PROTON THERAPY SYSTEM
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