Medical Device Recalls
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1 result found
510(K) Number: K091700 |
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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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VenaFlow Elite 30B-B and 30BI-B Product Usage: The VenaFlow Elite System is a compression pump ... | 2 | 07/03/2013 | DJO, LLC |
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