International Newtech Development, Inc.

International Newtech Development, Inc. — FDA 510(k) Submissions

International Newtech Development, Inc. has submitted 8 FDA 510(k) premarket notifications since 1995, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Visual, Pregnancy Hcg, Prescription Use, Single (specified) Analyte Controls (assayed And Unassayed), Kit, Test, Pregnancy, Hcg, Over The Counter, Diazo (colorimetric), Nitrite (urinary, Non-quant) . Use the specialty filter in the sidebar to narrow results.