Medical Device Recalls
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1 result found
510(K) Number: K100819 |
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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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| SOLOPATH Balloon Expandable TransFemoral System, Model Numbers STFI-1425, STFI-1435, STFI-1625, ... | 1 | 05/28/2019 |
FEI # 1118880 Terumo Medical Corporation |
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