Medical Device Recalls
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1 result found
510(K) Number: K180723 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| PreludeSYNC DISTAL Radial Compression Devices, SDRB-REG-LT, SDRB-REG-RT | 2 | 04/24/2020 |
FEI # 1721504 Merit Medical Systems, Inc. |
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