Carefusion 303, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Carefusion 303, Inc. has 7 FDA 510(k) cleared medical devices. Based in San Diego, US.
Latest FDA clearance: Apr 2025. Active since 2011. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Carefusion 303, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Carefusion 303, Inc.
7 devices
Cleared
Apr 25, 2025
BD Alaris Infusion System with Guardrails Suite MX
General Hospital
130d
Cleared
Jul 21, 2023
BD Alaris System with Guardrails Suite MX v12.1.2
General Hospital
819d
Cleared
Jul 19, 2017
MaxZero Extension Sets with Needless Connector
General Hospital
20d
Cleared
Jun 22, 2017
Multi-Link X2 ECG Adapter and Direct Connect Lead Wire System
Cardiovascular
211d
Cleared
Aug 21, 2014
ALARIS SYSTEM WITH GUARDRAILS SUITE MX
General Hospital
276d
Cleared
Mar 26, 2012
ALARIS PC UNIT MODULE 8000 WITH SOFTWARE CORRECTION
General Hospital
395d
Cleared
Jul 05, 2011
WIRELESS MONITORING SYSTEM
Cardiovascular
104d