Arrow International, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Arrow International, LLC - FDA 510(k) Cleared Devices
Recent clearances: AC3™ Range™ Intra-Aortic Balloon Pump, AC3™ Series IABP, Arrow 0.2 Micron Flat Filter, GVS
3
Total
3
Cleared
0
Denied
Arrow International, LLC has 3 FDA 510(k) cleared medical devices. Based in Morrisville, US.
Latest FDA clearance: Mar 2025. Active since 2023. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Arrow International, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Arrow International, LLC
3 devices