Medical Device Recalls
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1 result found
510(K) Number: K072521 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Vue Optic Visualization Source, Flexor Vue Deflecting Endoscopic System, Endoscope, Fiber Optic, Sup... | 2 | 06/05/2017 | Cook Inc. |
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