H&A Mui Enterprises, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
H&A Mui Enterprises, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PatCom Distal Chip Endoscope, PatCom Single-Use Introducer
2
Total
2
Cleared
0
Denied
H&A Mui Enterprises, Inc. has 2 FDA 510(k) cleared medical devices. Based in Mississauga, CA.
Last cleared in 2023. Active since 2020. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by H&A Mui Enterprises, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - H&A Mui Enterprises, Inc.
2 devices