Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K032338 |
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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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Trio Monitor. Cardiac Monitor (including cardiotachometer and rate alarm). | 2 | 10/13/2004 | Datascope Corp |
Trio Monitor. Cardiac Monitor (including cardiotachometer and rate alarm). | 2 | 09/21/2004 | Datascope Corp |
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