Medical Device Manufacturer · US , Sunrise , FL

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

9 submissions · 9 cleared · Since 2016

Total

Cleared

Denied

Inneuroco, Inc. has 9 FDA 510(k) cleared medical devices. Based in Sunrise, US.

Last cleared in 2023. Active since 2016. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Inneuroco, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Inneuroco, Inc.

9 devices

1-9 of 9

Cleared Sep 27, 2023

Thinline Sheath Introducer

K232260 · DYB

Cardiovascular · 58d

Cleared Jul 29, 2022

091 Balloon Guide Catheter

074 Zenith Flex System

Zenith Support, 95 cm, Zenith Support, 105 cm, Zenith Support, 115 cm

K173709 · DQY

Cardiovascular · 53d

Cleared Dec 06, 2017

091 Long Sheath, 70 cm, 091 Long Sheath, 80 cm, 091 Long Sheath, 90 cm

K172468 · DQY

Cardiovascular · 113d

Cleared Oct 19, 2017

065 Zenith, 074 Zenith

K171672 · DQY

Cardiovascular · 135d

Cleared Sep 19, 2016

Super Distal Access (SDA)

K161262 · DQY

Cardiovascular · 137d

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

FDA 510(k) cleared devices by Inneuroco, Inc.

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