Novalung GmbH is one of 22295 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Novalung GmbH - FDA 510(k) Cleared Devices
Recent clearances: NOVAPORT ONE VASCULAR ACCESS CANNULA, NOVALUNG SURGICAL LUNG ASSIST (SLA) MEMBRANE LUNG
2
Total
2
Cleared
0
Denied
Novalung GmbH has 2 FDA 510(k) cleared medical devices. Based in North Attleboro, US.
Historical record: 2 cleared submissions from 2007 to 2011. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Novalung GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Novalung GmbH
2 devices