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

STANDARD IMAGING E.IMRT CALCULATOR

K Number: K040688 · Decision May 11, 2004
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
255
Applicant Total
10
Review Days
56

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Basic Information

Device Name
STANDARD IMAGING E.IMRT CALCULATOR
K Number
K040688
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Standard Imaging, Inc.
Date Received
March 16, 2004
Decision Date
May 11, 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 Standard Imaging, Inc.

K Number Device Name
K103193 DOSEVIEW 3D
K082773 STANDARD IMAGING IMSURE BRACHY QA SOFTWARE, MODEL 91331
K060532 HDR 1000 PLUS WELL CHAMBER, MODEL 90008
K042733 STANDARD IMAGING PIPSPRO QA SOFTWARE SYSTEM
K013548 STANDARD IMAGING IVB 1000 WELL CHAMBER
K002833 MODIFICATION TO STANDARD IMAGING PT 1000 ION CHAMBER
K001825 STANDARD IMAGING HDR 1000 PLUS ION CHAMBER; STANDARD IMAGING IVB 1000 ION CHAMBER
K940539 STAND IMAGING DOSE CALIBRATOR SHIELDED WORK PLATFORM
K922554 STANDARD IMAGING HDR 1000 ION CHAMBER