Alfa Wassermann

Alfa Wassermann — FDA 510(k) Submissions

Alfa Wassermann has submitted 4 FDA 510(k) premarket notifications since 2012, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Nitrophenylphosphate, Alkaline Phosphatase Or Isoenzymes, Enzyme Immunoassay, Non-radiolabeled, Total Thyroxine, Nadh Oxidation/nad Reduction, Alt/sgpt, Enzymatic, Carbon-dioxide . Use the specialty filter in the sidebar to narrow results.