Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K050561 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Horizon Cardiology Hemo Component Schiller Argus Pro PB-1000 Monitor unit. Argus Pro PB 1000 firmwa... | 2 | 07/09/2010 | McKesson Provider Technologies - Medical Imaging Group |
Horizon Cardiology Hemo Monitoring System A programmable diagnostic computer intended for acquiri... | 2 | 06/24/2010 | McKesson Provider Technologies - Medical Imaging Group |
Horizon Cardiology Hemo Monitoring System;Horizon Cardiology Hemo External Control Unit;~100 - 230 V... | 2 | 02/05/2008 | McKesson Provider Technologies |
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