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

VIVIX-S 4386W (FXRD-4386WA)

K Number: K260820 · Decision Jun 18, 2026
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
422
Applicant Total
21
Review Days
97

Basic Information

Device Name
VIVIX-S 4386W (FXRD-4386WA)
K Number
K260820
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vieworks Co., Ltd.
Date Received
March 13, 2026
Decision Date
June 18, 2026
Product Code
MQB
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
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

Similar 510(k) Clearances

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Other Clearances by Vieworks Co., Ltd.

K Number Device Name
K254092 Bellalun 2D (VDMS-1000S)
K251410 VXvue
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. →