Medical Device Manufacturer · US , Lake Forest , IL

Hospira, Inc. - FDA 510(k) Cleared Devices

45 submissions · 44 cleared · Since 2004

Official Website

45

Total

44

Cleared

0

Denied

FDA 510(k) Regulatory Record - Hospira, Inc. Cardiovascular ✕

8 devices

1-8 of 8

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