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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