Medical Device Recalls
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1 result found
510(K) Number: K192684 |
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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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| TERUMO HydroPearl Compressible Microspheres for Embolisation REF 8HP2S600 | 2 | 01/31/2024 |
FEI # 3013556777 MICROVENTION INC. |
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