FDA 510(k) Applications Submitted by Steve Pavlik

FDA 510(k) Number Submission Date Device Name Applicant
K233838 12/04/2023 Emprint Ablation System with Thermosphere Technology (Overall System Name); Emprint Ablation Generator (CAGEN1); Emprint Ablation Generator HP (CAGENHP); Emprint Ablation Pump (CAPUMP1); CovidienÖ Ablation Footswitch (RFASW); Emprint Reinforced Percutaneo Medtronic, Inc


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