Medical Device Recalls
-
1 to 3 of 3 Results
510(K) Number: K121328 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Agility. Version 3.0 of the Integrity interface and control software for the Elekta range of medica... | 2 | 03/06/2014 | Elekta, Inc. |
Integrity 3.0 Product Usage: The Agility multileaf collimator is indicated for use when addition... | 2 | 05/25/2013 | Elekta, Inc. |
Multileaf Collimator To be used for single or multiple fractions, delivered as static and/or dyna... | 2 | 09/10/2012 | Elekta, Inc. |
-