Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K071992 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| High-Definition 120 MultiLeaf Collimator, Medical charged-particle radiation therapy system; Softwar... | 2 | 08/02/2008 |
FEI # 2916710 Varian Medical Systems Oncology Systems |
| High-Definition 120 Multileaf Collimator HD 120 MLC is an accessory x-ray collimator designed to ... | 2 | 08/22/2011 |
FEI # 2916710 Varian Medical Systems, Inc. Oncology Systems |
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