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FDA 510(k), K020537, TL10 TENSYMETER BLOOD PRESSURE MONITORING SYSTEM
FDA 510(k), K020537, TL10 TENSYMETER BLOOD PRESSURE MONITORING SYSTEM
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510(K) Number: K020537
Device Name: TL10 TENSYMETER BLOOD PRESSURE MONITORING SYSTEM
Manufacturer: TENSYS MEDICAL, INC.
Device Classification Name: system, measurement, blood-pressure, non-invasive
Regulation Number: 870.1130
Classification Product Code: DXN
Date Received: 02/19/2002
Decision Date: 08/15/2002
Regulation Medical Specialty: Cardiovascular
Device Name: TL10 TENSYMETER BLOOD PRESSURE MONITORING SYSTEM
Manufacturer: TENSYS MEDICAL, INC.
Device Classification Name: system, measurement, blood-pressure, non-invasive
Regulation Number: 870.1130
Classification Product Code: DXN
Date Received: 02/19/2002
Decision Date: 08/15/2002
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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