Milesman S.L. is one of 21656 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Milesman S.L. - FDA 510(k) Cleared Devices
Recent clearances: MILESMAN PREMIUM
1
Total
1
Cleared
0
Denied
Milesman S.L. has 1 FDA 510(k) cleared medical devices. Based in Great Neck, US.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Milesman S.L. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Milesman S.L.
1 devices