Medical Device Manufacturer · US , Sunrise , FL

Inneuroco, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2016
9
Total
9
Cleared
0
Denied
FDA 510(k) Regulatory Record - Inneuroco, Inc. Neurology ✕
4 devices
1-4 of 4
Cleared Jul 29, 2022
091 Balloon Guide Catheter
K220331 · DQY
Neurology · 175d
Cleared Aug 02, 2019
046 Zenith Flex
K190338 · NRY
Neurology · 169d
Cleared Oct 25, 2018
074 Zenith Flex System
K181354 · NRY
Neurology · 156d
Cleared Apr 19, 2018
Zenith Flex System
K172167 · NRY
Neurology · 275d
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