FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

myAblation Guide (VC10A)

K Number: K253264 · Decision Jun 16, 2026
Classifications
1
FEI Numbers
7
Registration Numbers
7
Same Product Code
8
Applicant Total
31
Review Days
260

Basic Information

Device Name
myAblation Guide (VC10A)
K Number
K253264
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Siemens Healthcare GmbH
Date Received
September 29, 2025
Decision Date
June 16, 2026
Product Code
QTZ
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
QTZ Radiological Image Processing Software For Ablation Therapy Planning And Evaluation

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