Instrumentation Laboratory Company

Instrumentation Laboratory Company — FDA 510(k) Submissions

Instrumentation Laboratory Company has submitted 3 FDA 510(k) premarket notifications since 2023, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrode Measurement, Blood-gases (pco2, Po2) And Blood Ph, Test, Qualitative And Quantitative Factor Deficiency, Instrument, Coagulation, Automated . Use the specialty filter in the sidebar to narrow results.