Cirrus Diagnostics, Inc.

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

Cirrus Diagnostics, Inc. has submitted 10 FDA 510(k) premarket notifications since 1991, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Colorimeter, Photometer, Spectrophotometer For Clinical Use, Enzymatic Esterase--oxidase, Cholesterol, Radioimmunoassay, Thyroid-stimulating Hormone, Enzyme Immunoassay, Non-radiolabeled, Total Thyroxine, Radioimmunoassay, Thyroxine-binding Globulin . Use the specialty filter in the sidebar to narrow results.