Chronimed, Inc.

Chronimed, Inc. — FDA 510(k) Submissions

Chronimed, Inc. has submitted 5 FDA 510(k) premarket notifications since 1997, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Glucose Oxidase, Glucose, System, Test, Blood Glucose, Over The Counter, Test, Urine Leukocyte, Single (specified) Analyte Controls (assayed And Unassayed) . Use the specialty filter in the sidebar to narrow results.