Medical Device Recalls
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1 result found
510(K) Number: K134044 |
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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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CardioTek EP-TRACER Software V1.x and V2.0 The EP-TRACER System is an electrophysiology measureme... | 2 | 06/30/2017 | CardioTek BV |
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