Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K011255 |
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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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Stereotactic Circular Collimator - 3D Line stereotatic Hardware Accessories The device is part of... | 2 | 11/04/2013 | Elekta, Inc. |
Stereotactic Circular Collimator Product Usage: This device is intended to hold a patient's head... | 2 | 11/30/2011 | Elekta, Inc. |
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