Medical Device Recalls
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1 result found
510(K) Number: K021362 |
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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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LKT200 Perfusion Circuit, part of Lifeport Kidney Perfusion Transporter KTR - Product Usage: The cir... | 2 | 03/04/2020 | Organ Recovery Systems, Inc. |
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