Poonglim Pharmatech, Inc.

Poonglim Pharmatech, Inc. — FDA 510(k) Submissions

Poonglim Pharmatech, Inc. has submitted 6 FDA 510(k) premarket notifications since 2018, of which 6 received clearance as substantially equivalent to a predicate device.

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