Alternative Pioneering Research and Development is one of 5319 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 ...
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.
Alternative Pioneering Research and Development — FDA 510(k) Products and Clearance History
2 devices
Cleared
May 23, 2013
SANICLAVE 102, MODEL RS-SC-102
General Hospital
239d
Cleared
Jan 11, 2012
SANICLAVE 200
General Hospital
106d