Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K212837 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ProxiDiagnost N90- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref: (1)70610... | 2 | 02/09/2024 | Philips North America |
| ProxiDiagnost upgrade- A Multi-functional general Radiography and Fluoroscopy (R/F) system Ref:7061... | 2 | 02/09/2024 | Philips North America |
| ProxiDiagnost N90, Radiography and Fluoroscopy (R/F) system | 2 | 11/08/2023 | Philips North America Llc |
| Philips ProxiDiagnost N90 1.0 (Model 706100) and ProxiDiagnost N90 1.1 (Model 706110)- A multi-func... | 2 | 04/28/2023 | Philips North America Llc |
| ProxiDiagnost N90. radiography and fluoroscopy system | 2 | 07/12/2022 | Philips Medical Systems DMC GmbH |
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