GIS

Test, Fibrinogen

Product code
GIS
Device name
Test, Fibrinogen
Device class
Class 2
21 CFR
21 CFR 864.7340
Medical specialty
Hematology
Marketing pathway
510(K)
Flag
Third-party review eligible
510(k) clearances (all years, FDA)
13 (all years; only the last 3 years are listed here)
Official FDA classification page: GIS
Classification and pathway per current FDA publications. Data from openFDA (CC0).