Medical Device Recalls
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1 result found
510(K) Number: K772348 |
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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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| HUDSON RCI®, Variable Concentration, Large Volume Nebulizer, Catalog Number (REF) 1770 and 41770, Rx... | 2 | 12/28/2007 |
FEI # 3005747797 Teleflex Creek Dr |
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