Coagusense, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Coagusense, Inc. has 3 FDA 510(k) cleared medical devices. Based in Fremont, US.
Last cleared in 2022. Active since 2010. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Coagusense, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Coagusense, Inc.
3 devices
Cleared
Oct 05, 2022
Coag-Sense Prothrombin (PT) / INR Monitoring System for Patient Self-Testing
Hematology
399d
Cleared
Feb 21, 2019
Coag-Sense Prothrombin Time (PT) / INR Monitoring Device
Hematology
92d
Cleared
Apr 07, 2010
COAGUSENSE SELF-TEST PROTHROMBIN TIME/INR MONITORING SYSTEM
Hematology
174d