510(k) K253008

Device
maiLink
Applicant
Maihub Corp.
510(k) number
K253008
Product code
LLZ
Decision
Substantially Equivalent (SESE)
Decision date
2026-01-05
Date received
2025-09-19
Regulation
892.2050
Classification name
System, Image Processing, Radiological
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Gyungeun Park
Address
4f, 58, Baumoe-Ro 37-Gil, Seocho-Gu Seoul KR 06744 06744

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Related GUDID Devices

Primary DIBrandCompanyPublished
08809921370023maiLinkmaihub Corp.2026-01-21

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