Medical Device Recalls
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1 result found
510(K) Number: K021958 |
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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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| Bacchus brand Trellis® Plus, Peripheral Infusion System, 6.0 Fr Catalog Numbers: BAC TRR 006 140 ... | 2 | 07/20/2004 |
FEI # 3003243511 Bacchus Vascular Inc |
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