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FDA 510(k), K062282, MONEBO AUTOMATED ECG ANALYSIS AND INTERPRETATION SOFTWARE LIBRARY, VERSION 3.0
FDA 510(k), K062282, MONEBO AUTOMATED ECG ANALYSIS AND INTERPRETATION SOFTWARE LIBRARY, VERSION 3.0
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510(K) Number: K062282
Device Name: MONEBO AUTOMATED ECG ANALYSIS AND INTERPRETATION SOFTWARE LIBRARY, VERSION 3.0
Manufacturer: MONEBO TECHNOLOGIES, INC.
Device Classification Name: Electrocardiograph
Regulation Number: 870.2340
Classification Product Code: DPS
Date Received: 08/07/2006
Decision Date: 03/22/2007
Regulation Medical Specialty: Cardiovascular
Device Name: MONEBO AUTOMATED ECG ANALYSIS AND INTERPRETATION SOFTWARE LIBRARY, VERSION 3.0
Manufacturer: MONEBO TECHNOLOGIES, INC.
Device Classification Name: Electrocardiograph
Regulation Number: 870.2340
Classification Product Code: DPS
Date Received: 08/07/2006
Decision Date: 03/22/2007
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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