Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K022411 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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PrecisePLAN Treatment Planning System Intended use: To plan multiple beam radiation therapy treat... | 2 | 03/04/2011 | Elekta, Inc. |
PrecisePLAN Treatment Planning System To plan multiple beam radiation therapy treatments. | 2 | 03/02/2011 | Elekta, Inc. |
PrecisePLAN 2.10 Treatment Planning System | 2 | 04/16/2010 | Elekta, Inc. |
PrecisePLAN 2.15 Treatment Planning System. The product is used to plan multiple beam radiation ... | 2 | 03/16/2010 | Elekta, Inc. |
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