Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K022634 |
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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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Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 18S, 1/18 GA Flexcore Biops... | 2 | 02/05/2021 | Argon Medical Devices, Inc |
Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 19, 1/19 GA Flexcore Biops... | 2 | 02/05/2021 | Argon Medical Devices, Inc |
Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 18N, 1/18 GA Flexcore Biop... | 2 | 02/05/2021 | Argon Medical Devices, Inc |
Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 19S, 1/19 GA Flexcore Biop... | 2 | 02/05/2021 | Argon Medical Devices, Inc |
Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 18C, 1/18 GA Flexcore Biop... | 2 | 02/05/2021 | Argon Medical Devices, Inc |
Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 19N, 1/19 GA Flexcore Biop... | 2 | 02/05/2021 | Argon Medical Devices, Inc |
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