DFI Co., Ltd.

DFI Co., Ltd. — FDA 510(k) Submissions

DFI Co., Ltd. has submitted 4 FDA 510(k) premarket notifications since 2006, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Method, Enzymatic, Glucose (urinary, Non-quantitative), Automated Urinalysis System . Use the specialty filter in the sidebar to narrow results.