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FDA 510(k) Applications Submitted by InNeuroCo Inc.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K220331
02/04/2022
091 Balloon Guide Catheter
InNeuroCo Inc.
K181354
05/22/2018
074 Zenith Flex System
InNeuroCo Inc.
K232260
07/31/2023
Thinline Sheath Introducer
Inneuroco Inc.
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