Artsana S.P.A is one of 18972 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Artsana S.P.A - FDA 510(k) Cleared Devices
Recent clearances: Safe Block Pen Needle, ARTSANA PISTON AND INSULIN SYRINGES, ARTSANA PEN NEEDLES, ARTSANA INJECTION NEEDLES
3
Total
3
Cleared
0
Denied
Artsana S.P.A has 3 FDA 510(k) cleared medical devices. Based in Bristol, US.
Historical record: 3 cleared submissions from 2005 to 2016. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Artsana S.P.A Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Wood Burditt Group as regulatory consultant.
FDA 510(k) Regulatory Record - Artsana S.P.A
3 devices