Medical Device Manufacturer · US , Bedford , MA

Instrumentation Laboratory (IL) Co.

4 submissions · 4 cleared · Since 2024
4
Total
4
Cleared
0
Denied

Instrumentation Laboratory (IL) Co. — FDA 510(k) Submissions

Instrumentation Laboratory (IL) Co. has submitted 4 FDA 510(k) premarket notifications since 2024, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Instrument, Coagulation, Automated, Platelet Factor 4 Radioimmunoassay, System, Fibrinogen Determination, Activated Partial Thromboplastin . Use the specialty filter in the sidebar to narrow results.

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All4 Hematology 4