Medical Device Recalls
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1 result found
510(K) Number: K822864 |
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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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MX6160R1, Custom CIPER (Comprehensive Intracranial Presssure Evaluation and Relief) System. The prod... | 2 | 04/26/2006 | Medex Inc |
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