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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K974736
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Product Description
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Recall
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EndoReturn arterial cannula. The EndoReturn arterial cannula is indicated for patients undergoing c... 3 01/09/2004 Heartport Inc
EndoReturn arterial cannula. The EndoReturn arterial cannula is indicated for patients undergoing c... 3 01/09/2004 Heartport Inc
Introducer Sheath is indicated for patients requiring introduction of catheters. Introducer Sheath ... 3 01/09/2004 Heartport Inc
SoftClamp II arterial cannula is intended to deliver oxygenated blood for cardiopulmonary bypass dur... 3 01/09/2004 Heartport Inc
DirectFlow arterial cannula is intended to deliver oxygenated blood for cardiopulmonary bypass durin... 3 01/09/2004 Heartport Inc
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