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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.
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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