Ivwatch, LLC - FDA 510(k) Cleared Devices
Recent clearances: ivWatch® Model 400, ivWatch Model 400, ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor, Patient Cable
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Ivwatch, LLC General Hospital ✕
6 devices
Cleared
Mar 15, 2024
ivWatch® Model 400
General Hospital
98d
Cleared
Aug 24, 2022
ivWatch Model 400
General Hospital
30d
Cleared
Jul 02, 2020
ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor,...
General Hospital
303d
Cleared
Dec 22, 2016
ivWatch
General Hospital
107d
Cleared
Feb 11, 2016
ivWatch Model 400
General Hospital
56d
Cleared
Feb 13, 2015
ivWatch Model 400
General Hospital
171d