Medical Device Recalls
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1 result found
510(K) Number: K113706 |
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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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EndoWrist Stapler System User Manual Addendum and Wall Chart; The EndoWrist Stapler 45 System an... | 2 | 08/08/2014 | Intuitive Surgical, Inc. |
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