Medifirst Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Medifirst Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: MF SAFECATH
1
Total
1
Cleared
0
Denied
Medifirst Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Cheonan-Si, KR.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medifirst Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Wise Company, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Medifirst Co., Ltd.
1 devices