Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K200849 |
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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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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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