Haolang Medical USA Corporation

Haolang Medical USA Corporation — FDA 510(k) Submissions

Haolang Medical USA Corporation has submitted 3 FDA 510(k) premarket notifications since 2021, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Umbilical Artery, Catheter, Percutaneous, Catheter, Hemodialysis, Implanted . Use the specialty filter in the sidebar to narrow results.