Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K140775 |
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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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Turbo Elite Atherectomy Catheter. Models: 410-152, 410-154, 414-151, 414-159, 417-152, 417-156, 420-... | 2 | 11/28/2016 | Spectranetics Corporation |
Bridge Occlusion Balloon. Model: 590-001 Temporary vessel occlusion of the superior vena cava in ap... | 2 | 11/28/2016 | Spectranetics Corporation |
ELCA Coronary Atherectomy Catheter. Models: 110-001, 110-002, 110-004, 114-009, 117-016, 117-205, 12... | 2 | 11/28/2016 | Spectranetics Corporation |
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