Haemoscope Corp.

Haemoscope Corp. — FDA 510(k) Submissions

Haemoscope Corp. has submitted 7 FDA 510(k) premarket notifications since 1989, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Instrument, Coagulation, Automated, System, Multipurpose For In Vitro Coagulation Studies, System, Automated Platelet Aggregation, Activated Whole Blood Clotting Time . Use the specialty filter in the sidebar to narrow results.