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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K974393
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Recall
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MediPress pneumatic compression system, Half Leg-Segmental Gradient, Model #6102-S 2 05/15/2019 FEI # 3012316249
Compass Health Brands (Corporate Office)
MediPress pneumatic compression system Full Leg (Short)-Segmental Gradient, Model #6103S-S 2 05/15/2019 FEI # 3012316249
Compass Health Brands (Corporate Office)
MediPress pneumatic compression system Full Leg (Medium)-Segmental Gradient, Model #6103M-S 2 05/15/2019 FEI # 3012316249
Compass Health Brands (Corporate Office)
MediPress pneumatic compression system Full Leg (Long)-Segmental Gradient, Model #6103L-S 2 05/15/2019 FEI # 3012316249
Compass Health Brands (Corporate Office)
MediPress pneumatic compression system Full Arm (Short)-Segmental Gradient, Model #6104S-S 2 05/15/2019 FEI # 3012316249
Compass Health Brands (Corporate Office)
MediPress pneumatic compression system Full Arm (Medium)-Segmental Gradient, Model #6104M-S 2 05/15/2019 FEI # 3012316249
Compass Health Brands (Corporate Office)
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