Medical Device Manufacturer · US , Baltimore , MD

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

9 submissions · 9 cleared · Since 2012
9
Total
9
Cleared
0
Denied

FDA 510(k) cleared devices by Corindus, Inc. Cardiovascular ✕

9 devices
1-9 of 9
Cleared Jul 27, 2022
CorPath GRX System
K221464 · DXX
Cardiovascular · 69d
Cleared Dec 11, 2020
CorPath GRX System
K202275 · DXX
Cardiovascular · 122d
Cleared Mar 29, 2018
CorPath GRX System
K180517 · DXX
Cardiovascular · 30d
Cleared Mar 01, 2018
CorPath GRX System
K173806 · DXX
Cardiovascular · 76d
Cleared Feb 15, 2018
CorPath GRX System
K173288 · DXX
Cardiovascular · 122d
Cleared Oct 27, 2016
CorPath GRX System
K160121 · DXX
Cardiovascular · 282d
Cleared Mar 18, 2016
CorPath 200 System
K152999 · DXX
Cardiovascular · 157d
Cleared Oct 02, 2015
CorPath 200 System
K150892 · DXX
Cardiovascular · 183d
Cleared Jul 19, 2012
CORPATH 200 SYSTEM
K120834 · DXX
Cardiovascular · 122d
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