Medical Device Recalls
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1 result found
510(K) Number: K113541 |
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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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INTIO Inc., ClearStart-SVM Segmentation and Volumetric Measurement System, Users Manual. Part #: UM... | 2 | 03/20/2013 | Intio Inc |
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