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FDA 510(k), K130773, TEMPUS PRO PATIENT MONITOR
FDA 510(k), K130773, TEMPUS PRO PATIENT MONITOR
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510(K) Number: K130773
Device Name: TEMPUS PRO PATIENT MONITOR
Manufacturer: REMOTE DIAGNOSTIC TECHNOLOGIES LTD.
Device Classification Name: monitor, physiological, patient (without arrhythmia detection or alarms)
Regulation Number: 870.2300
Classification Product Code: MWI
Date Received: 03/20/2013
Decision Date: 06/05/2013
Regulation Medical Specialty: Cardiovascular
Device Name: TEMPUS PRO PATIENT MONITOR
Manufacturer: REMOTE DIAGNOSTIC TECHNOLOGIES LTD.
Device Classification Name: monitor, physiological, patient (without arrhythmia detection or alarms)
Regulation Number: 870.2300
Classification Product Code: MWI
Date Received: 03/20/2013
Decision Date: 06/05/2013
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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