510(k) K241996

Device
ULTRA 1040
Applicant
Ecoray Co., Ltd.
510(k) number
K241996
Product code
IZL
Decision
Substantially Equivalent (SESE)
Decision date
2025-04-18
Date received
2024-07-09
Regulation
892.1720
Classification name
System, X-Ray, Mobile
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Haeri Lee
Address
58, Wangsimni-Ro, Seongdong-Gu #714~716, Forhu B/D Seoul KR 04778 04778

FDA Registration Numbers

Source Documents

510(k) summary PDF

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