Medical Device Recalls
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1 result found
510(K) Number: K143457 |
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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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NeuroBlate System SideFire Select 2.2 mm Directional Laser Probe, Sterile EO. Model #s SFS000-01,SF... | 1 | 05/16/2016 | Monteris Medical Corp |
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