Medical Device Manufacturer · CA , Mississauga

H&A Mui Enterprises, Inc.

2 submissions · 2 cleared · Since 2020
2
Total
2
Cleared
0
Denied

H&A Mui Enterprises, Inc. — FDA 510(k) Submissions

H&A Mui Enterprises, Inc. has submitted 2 FDA 510(k) premarket notifications since 2020, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Endoscopic Access Overtube, Gastroenterology-urology, Nasopharyngoscope (flexible Or Rigid) . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Gastroenterology & Urology 1 Ear, Nose, Throat 1