FDA 510(k) Applications Submitted by Mr. Ian Broome

FDA 510(k) Number Submission Date Device Name Applicant
K233318 09/29/2023 AXIOS Stent and Electrocautery-Enhanced Delivery System (6mmx8mm); AXIOS Stent and Electrocautery-Enhanced Delivery System (8mmx8mm); AXIOS Stent and Electrocautery-Enhanced Delivery System (10mmx10mm); AXIOS Stent and Electrocautery-Enhanced Delivery Sys Boston Scientific Corporation


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