Medical Device Recalls
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1 result found
510(K) Number: K110001 |
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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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The product is Pathfinder SL, version 1.6.0.3057 software used with the Spacelabs Healthcare Pathfin... | 2 | 06/20/2012 | Spacelabs Healthcare, Llc |
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