Home / 510(k) Clearances / K161113

510(k) K161113

QXLink by Vieworks Co., Ltd. — Product Code LLZ

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 5, 2016
Date Received
April 20, 2016
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Image Processing, Radiological
Device Class
Class II
Regulation Number
892.2050
Review Panel
RA
Submission Type

Other clearances by Vieworks Co., Ltd.

  • K251410 — VXvue (November 4, 2025)
  • K241113 — VIVIX-M (January 16, 2025)
  • K241125 — VIVIX-S 1751S (November 15, 2024)
  • K220239 — Solid State X-ray Imager(Model: FXRD-4386WB) (September 13, 2022)
  • K221512 — Vivix-S FW (Model: FXRD-2530FAW, FXRD-3643FAW, FXRD-4343FAW) (July 20, 2022)
  • K200418 — VIVIX-S VW (March 18, 2020)
  • K190611 — VIVIX-S 1751S (April 8, 2019)
  • K181003 — VIVIX-S 1717V (May 15, 2018)
  • K163703 — VIVIX-S 1417N (February 8, 2017)
  • K152894 — VIVIX-S 1717N (February 26, 2016)

Other clearances for product code LLZ

  • K260479 — TheraSphere 360™ Y-90 Management Platform (March 13, 2026)
  • K253111 — Aeka Imaging (March 13, 2026)
  • K251964 — Mimics Thoracic Planner (March 12, 2026)
  • K253551 — VELYS™ Hip Navigation (March 6, 2026)
  • K253486 — SKIA-Head (Model: SKIA-ST00) (February 23, 2026)
  • K260205 — AS Software Version Asera (February 19, 2026)
  • K253927 — LiveMedica Enterprise PACS (February 6, 2026)
  • K251577 — LAIA XR (February 6, 2026)
  • K253639 — View (January 8, 2026)
  • K253784 — 3DICOM MD Cloud (January 8, 2026)