Medical Device Recalls
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1 result found
510(K) Number: K072232 |
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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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Polyflux Revaclear, Capillary Dialyzer, Model Number 110633; Gambro Renal Products, Inc. Intende... | 2 | 05/21/2014 | Gambro Renal Products, Incorporated |
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