Medical Device Recalls
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1 result found
510(K) Number: K120855 |
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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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Philips IntelliSpace ECG Management System, with software option C61 needed to import ECGs from the... | 2 | 08/21/2014 | Philips Medical Systems, Inc. |
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