FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

myray ProXIma X6

K Number: K252353 · Decision Mar 10, 2026
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
133
Applicant Total
21
Review Days
224

Basic Information

Device Name
myray ProXIma X6
K Number
K252353
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cefla S.C.
Date Received
July 29, 2025
Decision Date
March 10, 2026
Product Code
OAS
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
OAS X-Ray, Tomography, Computed, Dental

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