Jiangsu Caina Medical Co.,Ltd

Jiangsu Caina Medical Co.,Ltd — FDA 510(k) Submissions

Jiangsu Caina Medical Co.,Ltd has submitted 21 FDA 510(k) premarket notifications since 2018, of which 21 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Needle, Hypodermic, Single Lumen, Enteral Syringes With Enteral Specific Connectors, Syringe, Antistick, Tubes, Vials, Systems, Serum Separators, Blood Collection, Syringe, Piston . Use the specialty filter in the sidebar to narrow results.