Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K160583 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Refinity Short Tip Rotational Intravascular Ultrasound (IVUS) Catheter; Product number: 400-0200.27... | 2 | 04/10/2017 | Volcano Corporation |
| Refinity Rotational Intravascular Ultrasound (IVUS) Catheter; Product number: 400-0200.289; Catalog... | 2 | 04/10/2017 | Volcano Corporation |
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