Medical Device Recalls
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1 result found
510(K) Number: K150958 |
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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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| LIFEPEARL Drug Elutable Microspheres: 200 +/- 50 micrometers, REF: 8LP2S200; 400 +/- 50 micrometers,... | 2 | 07/28/2025 |
FEI # 3013556777 MICROVENTION INC. |
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