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FDA 510(k), K013478, DYNAPULSE 5200A PATHWAY BLOOD PRESSURE MONITORING SYSTEM
FDA 510(k), K013478, DYNAPULSE 5200A PATHWAY BLOOD PRESSURE MONITORING SYSTEM
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510(K) Number: K013478
Device Name: DYNAPULSE 5200A PATHWAY BLOOD PRESSURE MONITORING SYSTEM
Manufacturer: PULSE METRIC, INC.
Device Classification Name: system, measurement, blood-pressure, non-invasive
Regulation Number: 870.1130
Classification Product Code: DXN
Date Received: 10/19/2001
Decision Date: 01/10/2002
Regulation Medical Specialty: Cardiovascular
Device Name: DYNAPULSE 5200A PATHWAY BLOOD PRESSURE MONITORING SYSTEM
Manufacturer: PULSE METRIC, INC.
Device Classification Name: system, measurement, blood-pressure, non-invasive
Regulation Number: 870.1130
Classification Product Code: DXN
Date Received: 10/19/2001
Decision Date: 01/10/2002
Regulation Medical Specialty: Cardiovascular
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
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