Accumetrics, Inc.

Accumetrics, Inc. — FDA 510(k) Submissions

Accumetrics, Inc. has submitted 7 FDA 510(k) premarket notifications since 1999, of which 7 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Automated Platelet Aggregation . Use the specialty filter in the sidebar to narrow results.