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

TOMOTHERAPY TREATMENT SYSTEM FAST OPTIMIZER

K Number: K112776 · Decision Dec 22, 2011
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
255
Applicant Total
6
Review Days
87

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Basic Information

Device Name
TOMOTHERAPY TREATMENT SYSTEM FAST OPTIMIZER
K Number
K112776
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Tomotherapy Incorporated
Date Received
September 26, 2011
Decision Date
December 22, 2011
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 Tomotherapy Incorporated

K Number Device Name
K112446 TOMOTHERAPY TREATMENT SYSTEM
K082005 MODIFICATION TO HI-ART TREATMENT SYSTEM
K060912 MODIFICATION TO: HI-ART SYSTEM
K042739 HI-ART SYSTEM
K033347 MODIFICATION TO: HI-ART SYSTEM