Medical Device Recalls
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1 result found
510(K) Number: K070157 |
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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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OmniGuide BP-ROBOTIC ( BeamPath Robotic), Single Use Cat. # BP-ROBOTIC The OmniGuide Fiber is in... | 2 | 12/03/2012 | OmniGuide, Inc. |
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