Clearflow, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Clearflow, Inc. has 6 FDA 510(k) cleared medical devices. Based in Anaheim, US.
Last cleared in 2021. Active since 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Clearflow, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Clearflow, Inc.
6 devices
Cleared
Mar 02, 2021
PleuraFlow System with FlowGlide
General & Plastic Surgery
104d
Cleared
Jul 26, 2019
The ZIP Accessory Shuttle for PleuraFlow System
General & Plastic Surgery
28d
Cleared
Aug 14, 2018
PleuraFlow System with FlowGlide Extra Drainage Length
General & Plastic Surgery
13d
Cleared
Nov 30, 2016
PleuraFlow System with FlowGlide
General & Plastic Surgery
21d
Cleared
Jan 20, 2016
PleuraFlow System
General & Plastic Surgery
29d
Cleared
Jun 02, 2015
PleuraFlow System
General & Plastic Surgery
144d