Medical Device Recalls
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1 result found
510(K) Number: K020862 |
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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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Eclipse Infusion Pump, 250 ml X 250 ml per hour) Part 5001247 | 2 | 01/09/2004 | I-Flow Corporation |
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