Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K201746 |
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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 Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-1004, and 00... | 2 | 09/21/2023 | Remote Diagnostic Technologies Ltd. |
Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by clinicians and m... | 2 | 04/01/2023 | Remote Diagnostic Technologies Ltd. |
Tempus Pro - Patient physiological monitor, arrhythmia detector and alarm. Part No. - 00-1004-R, 0... | 2 | 07/01/2021 | Remote Diagnostic Technologies Ltd. |
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