Interlab S.R.L.

Interlab S.R.L. — FDA 510(k) Submissions

Interlab S.R.L. has submitted 4 FDA 510(k) premarket notifications since 2003, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Analysis, Electrophoretic Hemoglobin, Immunoelectrophoretic, Immunoglobulins, (g, A, M), Abnormal Hemoglobin Quantitation . Use the specialty filter in the sidebar to narrow results.