Accriva Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
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
Accriva Diagnostics, Inc. has 3 FDA 510(k) cleared medical devices. Based in San Diego, US.
Last cleared in 2023. Active since 2019. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Accriva Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Accriva Diagnostics, Inc.
3 devices