510(k) K230461
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 24, 2023
- Date Received
- February 21, 2023
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Coagulation System For The Measurement Of Whole Blood Viscoelastic Properties
- Device Class
- Class II
- Regulation Number
- 864.5430
- Review Panel
- HE
- Submission Type
A coagulation system for the measurement of whole blood viscoelastic properties is an in vitro diagnostic device used to evaluate blood coagulation, fibrinolysis, or both, in patients.