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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K010744
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Flowtron Trio DVT Pump; an Rx intermittent pneumatic compression deep vein thrombosis pump; ArjoHunt... 2 12/27/2012 FEI # 1419652
Arjo, Inc. dba ArjoHuntleigh
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