Coagusense, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
FDA 510(k) cleared devices by Coagusense, Inc. Hematology ✕
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