MDS Canada Inc. DBA MDS Nordion
8 FDA 510(k) clearances · Recalling firm
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| Record | Firm | Date |
|---|---|---|
| TheraSphere Administration Set (Part Number K125914-034). TheraSphere is indicated for rad recall (Z-1325-2009) | MDS Canada Inc. DBA MDS Nordion | 2009-06-05 |
| Theratron 780C Cobalt Radiotherapy recall (Z-1178-06) | MDS Canada Inc. DBA MDS Nordion | 2006-06-27 |
| Theratron 780E Cobalt Radiotherapy recall (Z-1179-06) | MDS Canada Inc. DBA MDS Nordion | 2006-06-27 |
| Theratron 1000 Cobalt Radiotherapy recall (Z-1180-06) | MDS Canada Inc. DBA MDS Nordion | 2006-06-27 |
| Theratron 1000E Cobalt Radiotherapy recall (Z-1181-06) | MDS Canada Inc. DBA MDS Nordion | 2006-06-27 |
| Theratron Phoenix Cobalt Radiotherapy recall (Z-1182-06) | MDS Canada Inc. DBA MDS Nordion | 2006-06-27 |
| Theratron Elite 80 Cobalt Radiotherapy recall (Z-1183-06) | MDS Canada Inc. DBA MDS Nordion | 2006-06-27 |
| Theratron Elite 100 Cobalt Radiotherapy recall (Z-1184-06) | MDS Canada Inc. DBA MDS Nordion | 2006-06-27 |
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Every clearance here is in the API, with alerts when new ones post.