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Intronix Technologies Obtains FDA 510(k) Clearance for Myoguide SystemIntronix has


Intronix Technologies Obtains FDA 510(k) Clearance for Myoguide System
Intronix has won US regulatory clearance for its Myoguide device with support from Emergo Group(PRWEB) February 01, 2012 Intronix Technologies Corporation, a Bolton, Ontario-based medical technology developer, has been granted 510(k) clearance by the US Food and Drug Administration (FDA) for its Myoguide injection site targeting system.A hand-held, battery-operated device, Myoguide functions by ...
 

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