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

ClearCalc Model RADCA V2.6

K Number: K252863 · Decision Dec 19, 2025
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
255
Applicant Total
14
Review Days
101

Basic Information

Device Name
ClearCalc Model RADCA V2.6
K Number
K252863
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Radformation, Inc.
Date Received
September 9, 2025
Decision Date
December 19, 2025
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

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Other Clearances by Radformation, Inc.

K Number Device Name
K253962 ClearCheck (RADCC V2.7)
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K252988 ChartCheck (RADCH V1.6)
K242729 AutoContour (Model RADAC V4)
K230685 AutoContour Model RADAC V3
K220598 AutoContour Model RADAC V2
K220583 ClearCheck Model RADCC V2
K220582 ClearCalc Model RADCA V2
K200323 AutoContour
K201119 ChartCheck
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