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BRIEF-Teleflex receives FDA 510(k) clearance for Arrow AC3 Optimustm Intra-Aortic Balloon Pump
May 2, 2017 / 11:17 AM / 7 months ago

BRIEF-Teleflex receives FDA 510(k) clearance for Arrow AC3 Optimustm Intra-Aortic Balloon Pump

May 2 (Reuters) - Teleflex Inc

* Teleflex receives fda 510(k) clearance for the arrow® ac3 optimustm intra-aortic balloon pump (iabp)

* Teleflex receives fda 510(k) clearance for the arrow® ac3 optimustm intra-aortic balloon pump (iabp)

* Teleflex inc- ac3 optimus iabp will be launched at two scientific meetings in may Source text for Eikon: Further company coverage:

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