Quipu S.R.L is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Quipu S.R.L - FDA 510(k) Cleared Devices
Recent clearances: Cardiovascular Suite 4.2.1
1
Total
1
Cleared
0
Denied
Quipu S.R.L has 1 FDA 510(k) cleared medical devices. Based in Pisa, IT.
Last cleared in 2022. Active since 2022. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Quipu S.R.L Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Thomas Regulatory Resolutions, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Quipu S.R.L
1 devices