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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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