Wallac Oy, A Subsidiary of Perkinelmer, Inc. is one of 13096 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Wallac Oy, A Subsidiary of Perkinelmer, Inc. - FDA 510(k) Cleared Dev...
Recent clearances: GSP NEONATAL TOTAL GALACTOSE KIT, AUTODELFIA NEONATAL IRT KIT, GSP NEONATAL THYROXINE (T4)
3
Total
3
Cleared
0
Denied
Wallac Oy, A Subsidiary of Perkinelmer, Inc. has 3 FDA 510(k) cleared medical devices. Based in Waltham, US.
Historical record: 3 cleared submissions from 2011 to 2014. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Wallac Oy, A Subsidiary of Perkinelmer, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Wallac Oy, A Subsidiary of Perkinelmer, Inc.
3 devices