Covidien anuncia la aprobacin 510(k) de la FDA relativa al software de supervisin de la frecuencia respiratoria NellcorTM

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Covidien anuncia la aprobacin 510(k) de la FDA re .. upervisin de la frecuencia respiratoria NellcorTM

Covidien anuncia la aprobacin 510(k) de la FDA relativa al software de supervisin de la frecuencia respiratoria NellcorTM

^{Published on 2012-03-20 08:07:18 - Market Wire}

BOULDER, Colo.--([ BUSINESS WIRE ])--[ Covidien ] (NYSE: COV), proveedor lder internacional de productos sanitarios y reconocido innovador en el mbito de los equipos de supervisin de pacientes y de cuidados respiratorios, ha anunciado hoy que la Food and Drug Administration (FDA) de Estados Unidos ha concedido a la empresa la aprobacin 510(k) para la comercializacin del software de supervisin de la frecuencia respiratoria Covidien Nellcor^TM versin 1.0, y de su sensor de frecuencia respiratoria para adultos.

El comunicado en el idioma original, es la versin oficial y autorizada del mismo. La traduccin es solamente un medio de ayuda ydeber sercomparada con el texto en idioma original, que es la nica versin del texto que tendr validez legal.