VEINCAS vein finder Receives U.S. FDA Market Access License
Source: | Author:VEINCAS | vivolight | Published time: 2017-02-22 | 2086 Views | Share:

In February 2017, VEINCAS vein finder VIVO300 and VIVO500S successfully passed the US FDA market access license of the US Food and Drug Administration (FDA). This FDA certification marks that VEINCAS vein finder has been recognized by the US market in terms of technology, quality control and safety and reliability, and has opened up a channel for it to enter the North American market, marking the international Another big step forward on the road.


Enter 10054042, you can search the FDA approval information of Zhongke Weiguang on the FDA official website.