Alternative Pioneering Research and Development is one of 18945 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alternative Pioneering Research and Development - FDA 510(k) Cleared ...
Recent clearances: SANICLAVE 102, MODEL RS-SC-102, SANICLAVE 200
2
Total
2
Cleared
0
Denied
Alternative Pioneering Research and Development has 2 FDA 510(k) cleared medical devices. Based in Shafer, US.
Historical record: 2 cleared submissions from 2012 to 2013. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Alternative Pioneering Research and Development Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alternative Pioneering Research and Development
2 devices