FDA 510(k), K140847, CARDIOSPY ECG HOLTER SYSTEMS
FDA 510(k), K140847, CARDIOSPY ECG HOLTER SYSTEMS
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$149.00 USD
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510(K) Number: K140847
Device Name: CARDIOSPY ECG HOLTER SYSTEMS
Manufacturer:
Device Classification Name: Electrocardiograph, Ambulatory, With Analysis Algorithm
Regulation Number: 870.2800
Classification Product Code: MLO
Date Received: 04/03/2014
Decision Date: 12/05/2014
Regulation Medical Specialty: Cardiovascular
Device Name: CARDIOSPY ECG HOLTER SYSTEMS
Manufacturer:
Device Classification Name: Electrocardiograph, Ambulatory, With Analysis Algorithm
Regulation Number: 870.2800
Classification Product Code: MLO
Date Received: 04/03/2014
Decision Date: 12/05/2014
Regulation Medical Specialty: Cardiovascular