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FDA 510(k), K140933, ALIVECOR HEART MONITOR
FDA 510(k), K140933, ALIVECOR HEART MONITOR
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510(K) Number: K140933
Device Name: ALIVECOR HEART MONITOR
Manufacturer: ALIVECOR, INC.
Device Classification Name: Transmitters And Receivers, Electrocardiograph, Telephone
Regulation Number: 870.2920
Classification Product Code: DXH
Date Received: 04/11/2014
Decision Date: 08/15/2014
Regulation Medical Specialty: Cardiovascular
Device Name: ALIVECOR HEART MONITOR
Manufacturer: ALIVECOR, INC.
Device Classification Name: Transmitters And Receivers, Electrocardiograph, Telephone
Regulation Number: 870.2920
Classification Product Code: DXH
Date Received: 04/11/2014
Decision Date: 08/15/2014
Regulation Medical Specialty: Cardiovascular
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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