Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K900263 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Arrow Howes multi-lumen central venous catheterization kit 7 Fr x 20 cm | 3 | 11/01/2003 | Arrow International Inc |
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