Medical Device Recalls
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11 to 11 of 11 Results
510(K) Number: K100890 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Varian Medical Systems Inc., Millennium and HD-120 MultiLeaf Collimators (MLC), a component of the C... | 2 | 09/14/2011 | Varian Medical Systems, Inc. |
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