Mi MI Progress Co. , Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Mi MI Progress Co. , Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Mi MI Progress Co. , Ltd. has 3 FDA 510(k) cleared medical devices. Based in Buk-Gu, Daegu, KR.
Historical record: 3 cleared submissions from 1994 to 1995. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Mi MI Progress Co. , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mi MI Progress Co. , Ltd.
3 devices