Medical Device Recalls
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1 result found
510(K) Number: K102354 |
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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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| Grandio SO Heavy Flow Caps, Color A3 - Product Usage: Filling minimally invasive cavities of all cla... | 2 | 10/01/2019 |
FEI # 3002718942 Voco GmbH |
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