Medical Device Recalls
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1 result found
510(K) Number: K001633 |
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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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| LifeSite Hemodialysis Cannula Exchange Kit Part Number: LHCEK0000 | 3 | 10/15/2003 |
FEI # 3000719967 Vasca, Inc. |
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