Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K053584 |
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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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BrainLAB Target Positioner for Leksell Headring used with the iPlan RT Dose (versions 3.0, 3.0.1 and... | 2 | 07/03/2007 | Brainlab AG |
iPlan RT Dose is a stereotactic radiation treatment planning system that is intended for use in ster... | 2 | 01/15/2015 | Brainlab AG |
iPlan RT is a radiation treatment planning system that is intended for use in stereotactic, conforma... | 2 | 01/15/2015 | Brainlab AG |
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