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

ClearCheck (RADCC V2.7)

K Number: K253962 · Decision Apr 3, 2026
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
14
Review Days
113

Basic Information

Device Name
ClearCheck (RADCC V2.7)
K Number
K253962
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
December 11, 2025
Decision Date
April 3, 2026
Product Code
IYE
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
IYE Accelerator, Linear, Medical

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Other Clearances by Radformation, Inc.

K Number Device Name
K260509 AutoContour (RADAC V5)
K252988 ChartCheck (RADCH V1.6)
K252863 ClearCalc Model RADCA V2.6
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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