Master & Frank Enterprise Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Master & Frank Enterprise Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Master-Frank N95 Particulate Respirator
1
Total
1
Cleared
0
Denied
Master & Frank Enterprise Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Dong Duan, CN.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Master & Frank Enterprise Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shenzhen Joyantech Consulting Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Master & Frank Enterprise Co., Ltd.
1 devices