In-Line Diagnostics Corp.

In-Line Diagnostics Corp. — FDA 510(k) Submissions

In-Line Diagnostics Corp. has submitted 8 FDA 510(k) premarket notifications since 1995, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Hemodialysis, Access Recirculation Monitoring, Accessories, Blood Circuit, Hemodialysis, Device, Hematocrit Measuring, Instrument, Hematocrit, Automated . Use the specialty filter in the sidebar to narrow results.