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FDA 510(k), K063044, CARDIOBELT ELECTRODE BELT
FDA 510(k), K063044, CARDIOBELT ELECTRODE BELT
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$149.00 USD
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510(K) Number: K063044
Device Name: CARDIOBELT ELECTRODE BELT
Manufacturer: MONEBO TECHNOLOGIES, INC.
Device Classification Name: electrode, electrocardiograph
Regulation Number: 870.2360
Classification Product Code: DRX
Date Received: 10/04/2006
Decision Date: 03/23/2007
Regulation Medical Specialty: Cardiovascular
Device Name: CARDIOBELT ELECTRODE BELT
Manufacturer: MONEBO TECHNOLOGIES, INC.
Device Classification Name: electrode, electrocardiograph
Regulation Number: 870.2360
Classification Product Code: DRX
Date Received: 10/04/2006
Decision Date: 03/23/2007
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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