Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K991054 |
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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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NicoletOne version 5.20 software (also known as NicoletOne Version 5.2 Software) used with the Nicol... | 3 | 02/15/2007 | Nicolet Biomedical Div of Viasys Healthcare |
NicoletOne photic adapter cable 085-463700 | 2 | 09/21/2008 | Cardinal Health NeuroCare Division |
NicoletOne 5.30.2 Software when used with CSeries amplifiers in Fixed Room LTM Configurations with ... | 2 | 09/23/2008 | Cardinal Health NeuroCare Division |
NicoletOne vEEG System, VIASYS Healthcare, Inc., Madison, Wisconsin 53711. | 2 | 04/07/2010 | CareFusion |
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