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

VXvue

K Number: K251410 · Decision Nov 4, 2025
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
21
Review Days
181

Basic Information

Device Name
VXvue
K Number
K251410
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vieworks Co., Ltd.
Date Received
May 7, 2025
Decision Date
November 4, 2025
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LLZ), ordered by most recent decision date.

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Other Clearances by Vieworks Co., Ltd.

K Number Device Name
K260820 VIVIX-S 4386W (FXRD-4386WA)
K254092 Bellalun 2D (VDMS-1000S)
K241113 VIVIX-M
K241125 VIVIX-S 1751S
K220239 Solid State X-ray Imager(Model: FXRD-4386WB)
K221512 Vivix-S FW (Model: FXRD-2530FAW, FXRD-3643FAW, FXRD-4343FAW)
K200418 VIVIX-S VW
K190611 VIVIX-S 1751S
K181003 VIVIX-S 1717V
K163703 VIVIX-S 1417N
Search all 21 clearances from Vieworks Co., Ltd. →