Medical Device Manufacturer · US , Washington , DC

Nordion International, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1995

Recent clearances: GAMMACELL 3000 ELAN, VERSION 1.0 AND GAMMACELL 1000 ELITE, VERSION 1.0, GAMMACELL 3000 ELAN

View 2 510(k) Devices ↓

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Nordion International, Inc. Radiology ✕

2 devices

1-2 of 2

Cleared Nov 08, 1996

GAMMACELL 3000 ELAN, VERSION 1.0 AND GAMMACELL 1000 ELITE, VERSION 1.0

Radiology · 66d

Cleared Aug 25, 1995

GAMMACELL 3000 ELAN

Radiology · 101d