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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.
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