Medical Device Recalls
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1 result found
510(K) Number: K070947 |
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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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INTUITIVE SURGICAL DA VINCI SURGICAL SYSTEM, MODE; S Cardiac Probe Gasper Instrument, Model IS2000, ... | 2 | 09/17/2008 | Intuitive Surgical, Inc. |
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