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

Hybrid Viewer (00859873006240)

K Number: K252477 · Decision Sep 9, 2025
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
470
Applicant Total
16
Review Days
33

Basic Information

Device Name
Hybrid Viewer (00859873006240)
K Number
K252477
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1200
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hermes Medical Solutions AB
Date Received
August 7, 2025
Decision Date
September 9, 2025
Product Code
KPS
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
KPS System, Tomography, Computed, Emission

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