FDA 510(k) Applications Submitted by CoaguSense, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K212779 | 09/01/2021 | Coag-Sense Prothrombin (PT) / INR Monitoring System for Patient Self-Testing | CoaguSense, Inc. |
| K183255 | 11/21/2018 | Coag-Sense Prothrombin Time (PT) / INR Monitoring Device | CoaguSense, Inc. |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact