FDA 510(k) Applications Submitted by Stephanie Reneau

FDA 510(k) Number Submission Date Device Name Applicant
K233341 09/29/2023 ShileyÖ Oral/Nasal Endotracheal Tube Intermediate Cuff, Non-DEHP (87430, 87435, 87440, 87445, 87450, 87455, 87460, 87465, 87470, 87475, 87480, 87485, 87490, 87495, 87410) Covidien LLC


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