North America BioPharma is one of 22741 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
Recent clearances: MEDICINAL LEECHES, MEDICINAL LEECHES
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.
Regulatory submissions have been managed by Ricarimpex Sas and Biopharm (Uk) , Ltd..
FDA 510(k) Regulatory Record - North America BioPharma
2 devices