North America BioPharma is one of 5643 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
North America BioPharma - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
North America BioPharma has 2 FDA 510(k) cleared medical devices. Based in Erie, US.
Historical record: 2 cleared submissions from 2004 to 2014. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by North America BioPharma Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - North America BioPharma
2 devices