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

EMLA (Elekta Evo); EMLA (VersaHD); EMLA (Elekta Harmony Pro); EMLA (Elekta Infintiy); EMLA (Elekta Harmony); EMLA (Elekta Synergy)

K Number: K252188 · Decision Jan 15, 2026
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
733
Applicant Total
14
Review Days
185

Basic Information

Device Name
EMLA (Elekta Evo); EMLA (VersaHD); EMLA (Elekta Harmony Pro); EMLA (Elekta Infintiy); EMLA (Elekta Harmony); EMLA (Elekta Synergy)
K Number
K252188
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Elekta Solutions AB
Date Received
July 14, 2025
Decision Date
January 15, 2026
Product Code
IYE
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
IYE Accelerator, Linear, Medical

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