Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K153729 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| FlowGate2 Balloon Guide Catheter, UPN 90485 (8Fx85cm size) and 90495 (8Fx95cm size) | 2 | 07/28/2018 | Stryker Neurovascular |
| FlowGate2 8F x 85cm, Catalog: 90485 FlowGate2 8F x 95cm, Catalog: 90495 | 2 | 05/28/2024 | Stryker Neurovascular |
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