510(k) K254092

Device
Bellalun 2D (VDMS-1000S)
Applicant
Vieworks Co., Ltd.
510(k) number
K254092
Product code
MUE
Decision
Substantially Equivalent (SESE)
Decision date
2026-05-28
Date received
2025-12-19
Regulation
892.1715
Classification name
Full Field Digital, System, X-Ray, Mammographic
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
Seonghwan Park
Address
41-3, Burim-Ro 170beon-Gil, Dongan-Gu Anyang-Si KR 14055 14055

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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