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FDA 510(k), K100763, MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL WATCH BP HOME N BP3MX1-4
FDA 510(k), K100763, MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL WATCH BP HOME N BP3MX1-4
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510(K) Number: K100763
Device Name: MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL WATCH BP HOME N BP3MX1-4
Manufacturer: MICROLIFE INTELLECTUAL PROPERTY GMBH
Device Classification Name: System, Measurement, Blood-Pressure, Non-Invasive
Regulation Number: 870.1130
Classification Product Code: DXN
Date Received: 03/17/2010
Decision Date: 08/27/2010
Regulation Medical Specialty: Cardiovascular
Device Name: MICROLIFE UPPER ARM AUTOMATIC DIGITAL BLOOD PRESSURE MONITOR, MODEL WATCH BP HOME N BP3MX1-4
Manufacturer: MICROLIFE INTELLECTUAL PROPERTY GMBH
Device Classification Name: System, Measurement, Blood-Pressure, Non-Invasive
Regulation Number: 870.1130
Classification Product Code: DXN
Date Received: 03/17/2010
Decision Date: 08/27/2010
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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