Simplicity Diagnostics, Inc.

Simplicity Diagnostics, Inc. — FDA 510(k) Submissions

Simplicity Diagnostics, Inc. has submitted 5 FDA 510(k) premarket notifications since 1992, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include C-reactive Protein, Antigen, Antiserum, And Control, Antistreptolysin - Titer/streptolysin O Reagent, System, Test, Rheumatoid Factor, System, Test, Infectious Mononucleosis, Kit, Serological, Positive Control . Use the specialty filter in the sidebar to narrow results.