Leocor, Inc.

Leocor, Inc. — FDA 510(k) Submissions

Leocor, Inc. has submitted 3 FDA 510(k) premarket notifications since 1990, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Echocardiograph, Catheter, Intravascular, Diagnostic, Withdrawal/infusion Pump . Use the specialty filter in the sidebar to narrow results.