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

ONCENTRA-VISIR

K Number: K041719 · Decision Jul 22, 2004
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
255
Applicant Total
27
Review Days
28

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Basic Information

Device Name
ONCENTRA-VISIR
K Number
K041719
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Nucletron Corp.
Date Received
June 24, 2004
Decision Date
July 22, 2004
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

Other 510(k) clearances with the same product code (MUJ), ordered by most recent decision date.

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Other Clearances by Nucletron Corp.

K Number Device Name
K092804 MICROSELECTRON HDR V2, MODEL 105.999
K091598 LUMENCATH APPLICATOR SET, MODELS 189. 795, 189.796, 189.797, 189.798, LUMENCATH CATHETERS
K072445 INTEGRATED BRACHYTHERAPY UNIT - DIGITAL
K041715 INTRACAVITARY MOULD APPLICATOR SET, MODEL 189.001
K041933 MICROSELECTRON PDR
K031158 SWIFT 2.0, MODEL 132.001
K031349 OTP 1.2
K021286 MICROSELECTRON HDR- GENIE AFTERLOADING SYSTEM, MODEL 105.989 FOR 115VOLT DEVICES AND 105.988 FOR 230VOLT DEVICES
K020015 IMPLANT GUIDANCE SYSTEM APPLICATOR SET
K010032 SEED SELECTRON MODEL V. 1.0
Search all 27 clearances from Nucletron Corp. →