Mckesson Information Solutions, LLC
Mckesson Information Solutions, LLC holds FDA 510(k) medical device clearance, cleared in 2011, with 5 FDA device recalls on record.
Top product codes for Mckesson Information Solutions, LLC
FDA recalls by Mckesson Information Solutions, LLC
- Z-0042-2015 — McKesson Cardiology" Hemo intended for complete physiological/hemodynamic monitoring, clinical data acquisition, medical image and data processing, and analytical assessment.
- Z-0093-2015 — McKesson Cardiology Hemo. McKesson Cardiology" Hemo is intended for complete physiological/hemodynamic monitoring, clinical data acquisition, medical image and data processing, and analytical assessment.
- Z-0976-2014 — Horizon Medical Imaging, Picture Archive Communication System (PACS).
- Z-0556-2014 — McKesson Radiology 12.0, Picture Archiving Communication System (PACSA).
- Z-2318-2013 — McKesson Horizon Medical Imaging (HMI) Radiological Image Processing System, product versions 4.6.1 to 11.6., is a medical image and information management application intended to receive, transmit, store, retrieve, display, print and process digital medical images, digital medical video, and associated medical information from medical imaging systems.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Mckesson Information Solutions, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.