Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K160785 |
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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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0.035"(.89mm)x150 cm guidewire. Model 114135150. Soft Tip 3.5cm. REF/UDI: 114135150/(01)208863330080... | 1 | 05/07/2020 | Argon Medical Devices, Inc |
0.035"(.89mm)x80 cm guidewire. Model 114135080. Soft Tip 3.5cm. REF/UDI: 114135080/(01)2088633330080... | 1 | 05/07/2020 | Argon Medical Devices, Inc |
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