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

ProKnow DS

K Number: K251363 · Decision Oct 8, 2025
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
14
Review Days
160

Basic Information

Device Name
ProKnow DS
K Number
K251363
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Elekta Solutions AB
Date Received
May 1, 2025
Decision Date
October 8, 2025
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

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K223233 Monaco RTP System
K222047 Leksell Gamma Knife Perfexion, Leksell Gamma Knife Icon, Leksell Gamma Knife - Elekta Esprit (New model variant)
K213787 Monaco RTP System
K212218 Advanced Algorithms for Treatment Management Applications (AATMA)
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