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Remote Diagnostic Technologies Ltd.

11 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Philips Tempus Pro Patient Monitor, REF: 00-1004, 00-1007, 00-1004-R, 00-1007-R, 00-1024-R recall (Z-1027-2026)Remote Diagnostic Technologies Ltd.2026-01-08
Inseego USB8 4G Dongle Kit, Part Number: 01-2298, which contains USB Flash Drive, Part Num recall (Z-2175-2025)Remote Diagnostic Technologies Ltd.2025-07-25
Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-10 recall (Z-1729-2025)Remote Diagnostic Technologies Ltd.2025-05-07
Tempus Pro Patient Monitor, REFs: 00-1004-R (Tempus Pro non-printer, IBP, without headset recall (Z-1666-2025)Remote Diagnostic Technologies Ltd.2025-04-24
Tempus LS-Manual Defibrillator Model 00-3020 The Tempus LS-Manual is a defibrillator that recall (Z-0557-2025)Remote Diagnostic Technologies Ltd.2024-11-26
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 when using Tempus LS-Manual U recall (Z-2028-2024)Remote Diagnostic Technologies Ltd.2024-06-06
Philips Tempus Pro Patient Monitor, REF: 00-1004-R, 00-1007-R, 00-1024-R, 00-1026-R, 00-10 recall (Z-2625-2023)Remote Diagnostic Technologies Ltd.2023-09-21
Philips Tempus LS-Manual Defibrillator, Part Number: 00-3020 recall (Z-1825-2023)Remote Diagnostic Technologies Ltd.2023-06-12
Tempus Pro Patient Monitor is a portable vital signs monitor intended to be used by clinic recall (Z-1321-2023)Remote Diagnostic Technologies Ltd.2023-04-01
Tempus LS - Manual Defibrillator, Model Number: 00-3020 Software Version: 1.3.4 - Product recall (Z-0564-2021)Remote Diagnostic Technologies Ltd.2020-12-11
TEMPUS IC PROFESSIONAL Patient Monitor, Part No. 00-1002, Manufactured by: Remote Diagnost recall (Z-2183-2011)Remote Diagnostic Technologies Ltd.2011-05-11

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Every clearance here is in the API, with alerts when new ones post.