Medical Device Recalls
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1 result found
510(K) Number: K080364 |
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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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FindrWIRZ Guidewire System Catalog# 40-05 Cardiology: The system is intended for use in the card... | 1 | 11/09/2016 | SentreHeart Inc |
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