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www.fdanews.com/articles/176192-fujifilm-launches-sonosite-sii-snags-ce-mark-and-fda-clearance

FujiFilm Launches SonoSite SII, Snags CE Mark and FDA Clearance

April 13, 2016

Fujifilm SonoSite has received CE marking and 510(k) clearance for its SonoSite SII ultrasound system.

The portable system can be used for regional anesthesia, vascular access and trauma applications. Additionally, it includes a touchscreen interface with a clinician-driven menu logic, according to the company.

The company introduced the first mountable ultrasound system in 2007, according to Brian Leck, company vice president of global direct sales. — Anisa Jibrell