Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K111576 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Abbott NT2000iX Radiofrequency (RF) generator, REF RFG-NT-2000, lesioning generator | 2 | 11/02/2023 |
FEI # 3005334138 Abbott |
| NeuroTherm NT2000iX Radiofrequency (RF) Generator, Model Number RFG-NT-2000 | 2 | 05/10/2021 |
FEI # 1000139754 Abbott Laboratories Inc. (St Jude Medical) |
| Radiofrequency Grounding Pad, REF RF-DGP-L | 2 | 12/10/2019 |
FEI # 3005334138 Abbott Medical |
| Neurotherm NT2000iX RF Generator Model Number: RFG-NT -2000iX | 2 | 04/09/2016 |
FEI # 3002953813 Neurotherm, Inc. |
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