Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K183040 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Philips Zenition 70, System code 718133 - Product Usage: The devices are used for radiological guida... | 2 | 05/08/2020 |
FEI # 1218950 Philips North America, LLC |
| Zenition 70, Model #718133 | 2 | 02/17/2022 |
FEI # 3002807880 PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. |
| Zenition 70. Product Code 718133. The devices are used for radiological guidance and visualization d... | 2 | 04/21/2025 |
FEI # 3016618143 Philips North America Llc |
| Zenition 70. The device is to be used in health care facilities both inside and outside the operatin... | 2 | 04/21/2025 |
FEI # 3000976525 Philips Medical Systems Nederland B.V. |
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