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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