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FDA 510(k), K173768, Tempus Pro Patient Monitor
FDA 510(k), K173768, Tempus Pro Patient Monitor
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$149.00 USD
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510(K) Number: K173768
Device Name: Tempus Pro Patient Monitor
Manufacturer: Remote Diagnostic Technologies Ltd.
Device Classification Name: monitor, physiological, patient(with arrhythmia detection or alarms)
Regulation Number: 870.1025
Classification Product Code: MHX
Date Received: 12/11/2017
Decision Date: 01/10/2018
Regulation Medical Specialty: Cardiovascular
Device Name: Tempus Pro Patient Monitor
Manufacturer: Remote Diagnostic Technologies Ltd.
Device Classification Name: monitor, physiological, patient(with arrhythmia detection or alarms)
Regulation Number: 870.1025
Classification Product Code: MHX
Date Received: 12/11/2017
Decision Date: 01/10/2018
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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