Tsk Laboratory International Japan KK

Tsk Laboratory International Japan KK — FDA 510(k) Submissions

Tsk Laboratory International Japan KK has submitted 2 FDA 510(k) premarket notifications since 2024, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Low Dead Space Needle, Single Lumen, Hypodermic, Ophthalmic Needle . Use the specialty filter in the sidebar to narrow results.