Nordion International, Inc. - FDA 510(k) Cleared Devices
Recent clearances: GAMMACELL 3000 ELAN, VERSION 1.0 AND GAMMACELL 1000 ELITE, VERSION 1.0
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Nordion International, Inc. Radiology ✕
2 devices