Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K200849 |
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Product Description
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Recall
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FDA Recall
Posting Date |
Recalling Firm
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| Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that can de... | 3 | 11/26/2024 | Remote Diagnostic Technologies Ltd. |
| Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempus LS-Manual User/Operat... | 2 | 06/06/2024 | Remote Diagnostic Technologies Ltd. |
| Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 | 2 | 06/12/2023 | Remote Diagnostic Technologies Ltd. |
| Tempus LS - Manual Defibrillator, Model Number: 00-3020 Software Version: 1.3.4 - Product Usage: Th... | 2 | 12/11/2020 | Remote Diagnostic Technologies Ltd. |
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