Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K973628 |
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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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V-Twin, REF 6002-800 or 6002-850, SN 18-3304, IVD, (01)03661540600180 | 2 | 11/22/2019 | Vital Scientific N.V. |
Viva-E, Catalog # 6002-380, UDI # 03661540600050 Product Usage: automated chemistry analyzer in... | 2 | 10/16/2019 | Vital Scientific N.V. |
Viva - JR, catalog # 6002-940, UDI # 03661540600210 Product Usage: automated chemistry analyz... | 2 | 10/16/2019 | Vital Scientific N.V. |
V-Twin, Catalog # 6002-800, UDI # 03661540600180 Product Usage: automated chemistry analyzer in... | 2 | 10/16/2019 | Vital Scientific N.V. |
V-Twin, Catalog # 6002-800, UDI: 03661540600180 - Product Usage: An in vitro diagnostic device, whic... | 2 | 10/04/2019 | Vital Scientific N.V. |
V-Twin, Model # 6002-800, UDI: 03661540600180 Product Usage: An in-vitro diagnostic device, whic... | 2 | 09/23/2019 | Vital Scientific N.V. |
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