FDA 510(k) Applications Submitted by CAREFUSION 303, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K133532 11/18/2013 ALARIS SYSTEM WITH GUARDRAILS SUITE MX CAREFUSION 303, INC.
K243855 12/16/2024 BD Alaris Infusion System with Guardrails Suite MX CareFusion 303, Inc.
K163316 11/23/2016 Multi-Link X2 ECG Adapter and Direct Connect Lead Wire System CAREFUSION 303, INC.
K110809 03/23/2011 WIRELESS MONITORING SYSTEM CAREFUSION 303, INC.


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