Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K072502 |
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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 Muse v7 cardiology information system. Model number 2026443-001: MUSE 7.0 app cd, Mod... | 2 | 04/17/2013 | GE Healthcare, LLC |
GE Healthcare MUSE Cardiology Information Systems vs. 7.0, 7.0.1, 7.0.2, 7.1, 7.1.1. The MUSE Car... | 2 | 08/14/2009 | GE Healthcare, LLC |
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