FDA 510(k) Applications Submitted by Cerenovus, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K221930 07/01/2022 CEREGLIDE 71 Intermediate Catheter Cerenovus, Inc.
K221934 07/01/2022 CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set Cerenovus, Inc.
K241244 05/02/2024 CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter Cerenovus, Inc.
K230726 03/16/2023 CEREGLIDE 92 Intermediate Catheter Cerenovus, Inc.
K233988 12/18/2023 Cerenovus Large Bore Catheter; Cerenovus Aspiration Tubing Set Cerenovus, Inc.


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