Medical Device Recalls
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1 result found
510(K) Number: K060391 |
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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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Vacuum Source Tubing Set for the EndoWrist Stabilizer for da Vinci S (IS2000) and Si (IS3000); Part... | 2 | 02/27/2015 | Intuitive Surgical, Inc. |
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