Nasiff Assoc., Inc.

Nasiff Assoc., Inc. — FDA 510(k) Submissions

Nasiff Assoc., Inc. has submitted 5 FDA 510(k) premarket notifications since 1990, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Electrocardiograph, Monitor, Cardiac (incl. Cardiotachometer & Rate Alarm), System, Measurement, Blood-pressure, Non-invasive, LOS . Use the specialty filter in the sidebar to narrow results.