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FDA 510(k), K101123, NEXFIN MODEL 2
FDA 510(k), K101123, NEXFIN MODEL 2
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510(K) Number: K101123
Device Name: NEXFIN MODEL 2
Manufacturer: BMEYE B.V.
Device Classification Name: System, Measurement, Blood-Pressure, Non-Invasive
Regulation Number: 870.1130
Classification Product Code: DXN
Date Received: 04/22/2010
Decision Date: 10/28/2010
Regulation Medical Specialty: Cardiovascular
Device Name: NEXFIN MODEL 2
Manufacturer: BMEYE B.V.
Device Classification Name: System, Measurement, Blood-Pressure, Non-Invasive
Regulation Number: 870.1130
Classification Product Code: DXN
Date Received: 04/22/2010
Decision Date: 10/28/2010
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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