Medical Device Manufacturer · US , Portland , OR

Crestat Diagnostics, Inc. - FDA 510(k) Cleared Devices

29 submissions · 29 cleared · Since 1990

29

Total

29

Cleared

0

Denied

FDA 510(k) Regulatory Record - Crestat Diagnostics, Inc. Hematology ✕

3 devices

1-3 of 3

Cleared Oct 20, 1997

N-ASSAY TIA PLASMINOGEN TEST KIT

Hematology · 144d

Cleared Oct 20, 1997

N-ASSAY TIA ANTITHROMBIN III TEST KIT

Hematology · 125d

Cleared Apr 16, 1997

N-ASSAY TIA FIBRINOGEN TEST KIT

Hematology · 117d