Medical Device Recalls
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1 result found
510(K) Number: K022983 |
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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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| 1. X-Port isp M.R.I Implantable Port, with Pre-Attached 9.6 F Open-Ended Single-Lumen Venous Cathete... | 2 | 03/26/2020 |
FEI # 2020394 Bard Peripheral Vascular Inc |
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