The US FDA Grants 510(k) Clearance to Teleflex’s AC3 Range Intra-Aortic Balloon Pump (IABP) for Cardiac Patient Mobility
Shots:
- The US FDA has granted 510(k) clearance to the AC3 Range IABP, which will enter full market release in the US & begin shipping in Q2’25
- AC3 Range allows reliable IABP support during multiple pts transport modes, incl. ambulances & fixed or rotary-wing aircraft
- AC3 Range integrates the AC3 Optimus IABP’s interface & algorithms for precisely timed support, with features like full-size helium tank, dual power options, metal-reinforced handle, & four 360° swivel wheels for maneuverability to overcome transport-related challenges
Ref: Globenewswire | Image: Teleflex
Related News:- Teleflex Enters a Definitive Agreement to Acquire BIOTRONIK’s Vascular Intervention Business for ~$797.7M (€760M)
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Ridhi is an avid secondary researcher who follows trends in the biopharmaceutical and healthcare sectors to curate engaging content for the global audience. She works as a news editor at PharmaShots and loves to read books and explore new destinations.
