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Coagusense, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K212779 Coag-Sense Prothrombin (PT) / INR Monitoring System for Patient Self-TestingGJS2022-10-05 View
510(k) K183255 Coag-Sense Prothrombin Time (PT) / INR Monitoring DeviceGJS2019-02-21 View
510(k) K093243 COAGUSENSE SELF-TEST PROTHROMBIN TIME/INR MONITORING SYSTEMGJS2010-04-07 View
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