Gostar Co., Ltd.

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

Gostar Co., Ltd. has submitted 3 FDA 510(k) premarket notifications since 2023, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Meter, Peak Flow, Spirometry, Spirometer, Diagnostic, Multiple Use Blood Lancet For Single Patient Use Only . Use the specialty filter in the sidebar to narrow results.