Medequi, Division of King Yip Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medequi, Division of King Yip Co., Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Medequi, Division of King Yip Co., Inc. has 2 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Historical record: 2 cleared submissions from 1985 to 1985. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medequi, Division of King Yip Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medequi, Division of King Yip Co., Inc.
2 devices