510(k) K250597

Device
REMEX Xcam6
Applicant
Remedi, Inc.
510(k) number
K250597
Product code
IZL
Decision
Substantially Equivalent (SESE)
Decision date
2025-07-31
Date received
2025-02-28
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
No

Applicant Contact#

Contact
Seong-Geun Park
Address
#1408, Is Biz Tower Bldg. 1, 26 Yangpyeong-Ro 21 Gil 26, Yeongdeunpo-Gu, Yeongdeunpo-Gu Seoul KR 072NN 072NN

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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