ST. PAUL, Minn.--(BUSINESS WIRE)--Smiths Medical, a leading global medical device manufacturer, announced today it received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to launch ...
ST. PAUL, Minn.--(BUSINESS WIRE)--Smiths Medical, a leading global medical device manufacturer, announced today it has received FDA 510(k) clearance to market its CADD ®-Solis pain management system ...
ICU Medical Inc. a annoncé que la société avait reçu l'autorisation réglementaire 510(k) de la Food and Drug Administration (FDA) des États-Unis pour la pompe à perfusion Plum Duo avec le logiciel de ...
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