# Mckesson Israel, Ltd.

- Location (FDA's records): Tel Aviv, IL
- FDA decisions: 5 (2012–2015): 5 510(k) clearances
- Product codes: DQK (2), LLZ (2), MWI (1)
- Predicates its devices cite: 10 (2 its own); citations of its devices by later devices: 8 (2 its own)
- Recalls linked to its devices: 12 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medcon, Ltd.: 3 (https://510kreport.com/company/medcon)
- Ge Healthcare Integrated IT Solutions: 2 (https://510kreport.com/company/ge-healthcare-integrated-it-solutions)
- Philips Medical Systems North America, Inc.: 1 (https://510kreport.com/company/philips-medical-systems-north-america)
- Airstrip Technologies, LP: 1 (https://510kreport.com/company/airstrip-technologies)
- Witt Biomedical Corporation: 1 (https://510kreport.com/company/witt-biomedical)

## Firms that cite its devices most
- Fysicon BV: 2 (https://510kreport.com/company/fysicon)
- Change Healthcare Israel, Ltd.: 2 (https://510kreport.com/company/change-healthcare-israel)
- Carestream Health, Inc.: 1 (https://510kreport.com/company/carestream-health)
- Epiphany Healthcare, LLC: 1 (https://510kreport.com/company/epiphany-healthcare)

## Its most-cited devices
- K131497: Mckesson Cardiology Hemo (2013), cited by 3
- K133534: Mckesson Cardiology Ecg Mobile (2014), cited by 2
- K113515: Horizon Cardiology Ecg Management (2012), cited by 1
- K112720: Mckesson Horizon Cardiology (2012), cited by 1
- K151850: McKesson Cardiology (2015), cited by 1

## Recent decisions
- K151850: McKesson Cardiology (Aug 11, 2015)
- K133534: Mckesson Cardiology Ecg Mobile (Apr 18, 2014)
- K131497: Mckesson Cardiology Hemo (Dec 5, 2013)
- K113515: Horizon Cardiology Ecg Management (Mar 16, 2012)
- K112720: Mckesson Horizon Cardiology (Jan 30, 2012)

Source page: https://510kreport.com/company/mckesson-israel