FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

cvi42 Coronary Plaque Software Application

K Number: K251027 · Decision Oct 27, 2025
Classifications
1
FEI Numbers
217
Registration Numbers
217
Same Product Code
303
Applicant Total
9
Review Days
208

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Basic Information

Device Name
cvi42 Coronary Plaque Software Application
K Number
K251027
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Circle Cardiovascular Imaging, Inc.
Date Received
April 2, 2025
Decision Date
October 27, 2025
Product Code
QIH
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
QIH Automated Radiological Image Processing Software

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Other Clearances by Circle Cardiovascular Imaging, Inc.

K Number Device Name
K250221 StrokeSENS ASPECTS Software Application
K242781 cvi42 Software Application
K222593 TruPlan Computed Tomography (CT) Imaging Software
K213998 cvi42 Auto Imaging Software Application
K202212 TruPlan
K141480 CVI42
K111373 CT42 CARDIAC COMPUTED TOMOGRAPHY (CT) SOFTWARE
K082628 CMR42 CARDIAC MRI IMAGING SYSTEM, 2.1.23