Vieworks Co., Ltd.
FDA 510(k) medical device clearances.
Top product codes for Vieworks Co., Ltd.
Recent clearances by Vieworks Co., Ltd.
- 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
- K161113 — QXLink
- K152855 — VIVIX-S 1012N
- K152894 — VIVIX-S 1717N
- K132302 — QXLINK
- K122865 — VIVIX-S WIRELESS
- K122866 — VIVIX-S WITH VXVUE
- K120020 — VIVIX-S
- K092081 — QXLINK
- K080553 — DIGITAL RADIOGRAPHY SYSTEM, MODEL QXR-16
- K073056 — DIGITAL RADIOGRAPHY SYSTEM, MODEL: QXR-9
Data sourced from openFDA. This site is unofficial and independent of the FDA.