FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇪 Sweden

Voxel Dosimetry (00859873006226)

K Number: K243919 · Decision Jul 30, 2025
Classifications
1
FEI Numbers
217
Registration Numbers
217
Same Product Code
303
Applicant Total
16
Review Days
222

Basic Information

Device Name
Voxel Dosimetry (00859873006226)
K Number
K243919
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hermes Medical Solutions AB
Date Received
December 20, 2024
Decision Date
July 30, 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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K Number Device Name
K252477 Hybrid Viewer (00859873006240)
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K202882 Affinity
K193152 Affinity
K191216 Voxel Dosimetry™ v1.0
K181468 Hybrid3D
K171719 Hybrid3D
K171681 Hermes Medical Imaging Suite v5.7
K163687 OLINDA EXM
K163394 Hybrid3D
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