
Abiomed Receives 510(k) Clearance from FDA for Impella 2.5 Device
Abiomed Announces Results of Impella(R) 2.5 FDA PROTECT I Safety Trial for High-Risk PCI Cases
Abiomed Announces Schedule for TCT 2007 Global Live Broadcasts of Impella(R) 2.5 Patient Procedures
Abiomed Announces Update on Impella(R) 2.5 510(k) Process
Abiomed Receives Conditional FDA Approval for Impella 2.5 Pivotal Study at up to 150 Hospitals
Abiomed Announces Canadian Regulatory Approvals of Impella Circulatory Support Technologies
Abiomed Announces Schedule of Events for Breakthrough Impella Technology at EuroPCR Conference in Barcelona
Abiomed Completes Enrollment of Pilot Clinical Trial for Impella 2.5 Circulatory Support System
Abiomed's Impella 2.5 Circulatory Support System Receives Medical Design Excellence Award
Abiomed Expands Availability of Impella Circulatory Support Technologies with Regulatory Approvals in India
Abiomed Announces Data on Impella 2.5 for Improved Cardiac Function for Pre-Shock Acute Myocardial Infarction
Abiomed to Showcase Impella 2.5 Advanced Circulatory Support Technologies at American College of Cardiology's Annual Scientific Sessions
The Impella® is an Investigational Device limited by U.S. Federal Law solely for Investigational Use in the United States. |