Medical Device Recalls
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1 result found
510(K) Number: K060146 |
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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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ActiveCare +SFT Medical Compression Systems OR Aqiva, IL Intended for use in: Preventing deep V... | 2 | 01/11/2012 | Medical Compression Systems |
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