Medical Device Recalls
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1 result found
510(K) Number: K043581 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Gyrus ACMI 10 Fr. Dual Lumen Catheter Reference Number: 608 BX (Box of 5) and 608 (single unit) Th... | 2 | 09/16/2008 | Gyrus ACMI Corporation |
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