Accriva Diagnostics, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Tenderfoot, GEM Hemochron 100 System, GEM Hemochron 100 Activated Clotting Time Plus Test (ACT+), GEM Hemochron 100 Low Range Activated Clotting Time Test (ACT-LR), directCHECK ACT+ Whole Blood Control, Level 1 and Level 2, directCHECK ACT-LR Whole Blood Control, Level 1 and Level 2, Hemochron Signature Elite
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Accriva Diagnostics, Inc. General & Plastic Surgery ✕
1 devices