Hospira, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Plum 360(TM) Infusion System with MedNet/ Smart Card Plug and Play Module, Hospira Extension Set, Hospira Primary Set, Hospira Sapphire Sets
45
Total
44
Cleared
0
Denied
FDA 510(k) Regulatory Record - Hospira, Inc. Cardiovascular ✕
8 devices
Cleared
Sep 18, 2009
HOSPIRA LATEX-FREE CRITICAL CARE AND ADVANCED SENSOR CATHETERS
Cardiovascular
141d
Cleared
Mar 13, 2009
HOSPIRA VITAL SIGNS WIRELESS MONITORING SYSTEM
Cardiovascular
7d
Cleared
Nov 03, 2006
OPTICATH CENTRAL VENOUS OXIMETRY PROBE WITH SEAL WITH HEPARIN
Cardiovascular
32d
Cleared
Oct 05, 2006
OPTICATH CENTRAL VENOUS OXIMETRY CATHETER
Cardiovascular
120d
Cleared
Sep 19, 2006
TRANSPAC III DISPOSABLE STRAIGHT PRESSURE TRANSDUCER AND KIT
Cardiovascular
104d
Cleared
Aug 04, 2006
HOSPIRA LATEX-FREE ADVANCED SENSOR CATHETERS
Cardiovascular
71d
Cleared
Jun 26, 2006
OPTICATH CENTRAL VENOUS OXIMETRY PROBE WITH FLUIDIC SEAL WITH/WITHOUT HEPARIN
Cardiovascular
61d
Cleared
Feb 17, 2006
DISPOSABLE TRANSPAC III INTEGRATED TRANSDUCER (IT)
Cardiovascular
135d