Nemoto Kyorindo Co., Ltd.

Nemoto Kyorindo Co., Ltd. — FDA 510(k) Submissions

Nemoto Kyorindo Co., Ltd. has submitted 8 FDA 510(k) premarket notifications since 2005, of which 8 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Injector And Syringe, Angiographic, Injector, Contrast Medium, Automatic . Use the specialty filter in the sidebar to narrow results.