Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K021185 |
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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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Nicolet® Ambulatory EEG | 2 | 07/28/2018 | Natus Neurology Inc |
Viasys Healthcare NicoletOne ICU Monitor, Modular Neurodiagnostic System (containing Axiomtek Panel... | 3 | 01/03/2008 | Nicolet Biomedical Div of Viasys Healthcare |
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