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Heartport, Inc.

6 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
The Heartport EndoClamp aortic catheter is a 10.5 Fr. wirewound, three-lumen catheter with recall (Z-0811-05)Heartport, Inc.2005-05-10
EndoReturn arterial cannula. The EndoReturn arterial cannula is indicated for patients und recall (Z-0307-04)Heartport Inc2004-01-09
EndoReturn arterial cannula. The EndoReturn arterial cannula is indicated for patients und recall (Z-0308-04)Heartport Inc2004-01-09
DirectFlow arterial cannula is intended to deliver oxygenated blood for cardiopulmonary by recall (Z-0309-04)Heartport Inc2004-01-09
SoftClamp II arterial cannula is intended to deliver oxygenated blood for cardiopulmonary recall (Z-0310-04)Heartport Inc2004-01-09
Introducer Sheath is indicated for patients requiring introduction of catheters. Introduce recall (Z-0311-04)Heartport Inc2004-01-09

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Every clearance here is in the API, with alerts when new ones post.