Mckesson Israel , Ltd.
Mckesson Israel , Ltd. holds FDA 510(k) medical device clearances, first cleared 2012, most recent 2015, with 2 FDA device recalls on record.
Top product codes for Mckesson Israel , Ltd.
FDA recalls by Mckesson Israel , Ltd.
- Z-2968-2018 — McKesson Cardiology Hemo, Release SW version 13.0. Used for physiological monitoring, image and data processing. McKesson Cardiology Hemo is intended for complete physiological/hemodynamic monitoring, clinical data acquisition, medical image and data processing, and analytical assessment. McKesson Cardiology Hemo is also intended for patient/procedural data management, such as documentation, logging, reporting, trending, storing, reviewing, carrying out clinical calculations and exporting various representations of the acquired data.
- Z-0910-2015 — McKesson Cardiology ECG Management It is a software application designed to import, display, store, analyze, distribute and manage information related to ECG procedures of adult and pediatric patients from external ECG devices.
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 Israel , Ltd.
Data sourced from openFDA. This site is unofficial and independent of the FDA.