Medical Device Recalls
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11 to 12 of 12 Results
510(K) Number: K121398 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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HydroFinity Hydrophilic guidewire; 0.035 OD, Stiff Shaft, Straight Tip, 180 CM Length; Manufact... | 1 | 06/25/2014 | Nitinol Devices and Components, Inc. |
HydroFinity Hydrophilic guidewire; Nitinol Guidewire with Hydrophilic Coating, Sterile. 0.035 OD,... | 1 | 06/25/2014 | Nitinol Devices and Components, Inc. |
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