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FDA 510(k), K152701, Matrix Mini ECG Monitor
FDA 510(k), K152701, Matrix Mini ECG Monitor
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$149.00 USD
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$149.00 USD
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510(K) Number: K152701
Device Name: Matrix Mini ECG Monitor
Manufacturer: GLOBAL INSTRUMENTATION, LLC
Device Classification Name: detector and alarm, arrhythmia
Regulation Number: 870.1025
Classification Product Code: DSI
Date Received: 09/21/2015
Decision Date: 04/22/2016
Regulation Medical Specialty: Cardiovascular
Device Name: Matrix Mini ECG Monitor
Manufacturer: GLOBAL INSTRUMENTATION, LLC
Device Classification Name: detector and alarm, arrhythmia
Regulation Number: 870.1025
Classification Product Code: DSI
Date Received: 09/21/2015
Decision Date: 04/22/2016
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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