Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K050093 |
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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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GE Healthcare Systems ComboLab System. Made up of both Mac-Lab System, Software Version 6.5 202142... | 2 | 08/07/2007 | General Electric Medical Systems Information Technology |
GE Medical Systems CardioLab System, electrophysiological data system, Software Version 6.5 2021423-... | 2 | 08/07/2007 | General Electric Medical Systems Information Technology |
GE Medical Systems Mac-Lab System, cardiac catheterization data system. Software Version 6.5 202142... | 2 | 08/07/2007 | General Electric Medical Systems Information Technology |
Prucka 3 Amplifier Model #P1801PA used with CardioLab AltiX electrophysiology recording system and C... | 2 | 07/03/2024 | GE Medical Systems Information Technologies Inc |
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