FDA 510(k) FDA class 2 Substantially Equivalent 🇰🇷 South Korea

RAYMO Mobile X-ray System (Model: RAYMO)

K Number: K260085 · Decision May 14, 2026
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
235
Applicant Total
14
Review Days
122

Basic Information

Device Name
RAYMO Mobile X-ray System (Model: RAYMO)
K Number
K260085
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1720
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DRGEM Corporation
Date Received
January 12, 2026
Decision Date
May 14, 2026
Product Code
IZL
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
IZL System, X-Ray, Mobile

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