Haemonetics Corporation

Haemonetics Corporation — FDA 510(k) Submissions

Haemonetics Corporation has submitted 7 FDA 510(k) premarket notifications since 2016, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Multipurpose For In Vitro Coagulation Studies, Apparatus, Autotransfusion . Use the specialty filter in the sidebar to narrow results.