Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K152694 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Peripheral Diamondback 1.25 Solid OAD, a percutaneous orbital atherectomy system indicated for use a... | 2 | 10/11/2018 |
FEI # 3004742232 Cardiovascular Systems Inc |
| Peripheral Diamondback 1.50 Solid OAD, a percutaneous orbital atherectomy system indicated for use a... | 2 | 10/11/2018 |
FEI # 3004742232 Cardiovascular Systems Inc |
| DIAMONDBACK 360 Peripheral 1.50 Classic, Model DBP-150CLASS145 Peripheral Orbital Atherectomy Syste... | 2 | 02/22/2017 |
FEI # 3004742232 Cardiovascular Systems Inc |
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