Medical Device Recalls
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1 result found
510(K) Number: K182796 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| BD WAVELINQ 4F EndoAVF System, Arterial Catheter 50 cm, Venous Catheter 43 cm, Sterile EO, Rx only, ... | 2 | 04/02/2020 |
FEI # 2020394 Bard Peripheral Vascular Inc |
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