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FDA 510(k) Applications Submitted by Cerenovus Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K241221
05/01/2024
CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing Set
Cerenovus Inc.
K233982
12/18/2023
CEREGLIDE 92 Catheter System
Cerenovus Inc.
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