Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K080601 |
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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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Elekta ERGO++ Product Usage: ERGO is often used for stereotactic treatments. | 2 | 12/13/2017 | Elekta Inc |
ERGO++ Stereotactic Radiation Treatment Planning System, ERGO++ Release 1.6.3 and 1.6.3.1 Product... | 2 | 06/23/2011 | Computerized Medical Systems Inc |
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