FDA 510(k), K082870, VTI INTRAOPERATIVE DOPPLER SYSTEMS

FDA 510(k), K082870, VTI INTRAOPERATIVE DOPPLER SYSTEMS

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510(K) Number: K082870
Device Name: VTI INTRAOPERATIVE DOPPLER SYSTEMS
Manufacturer:
Device Classification Name: Flowmeter, Blood, Cardiovascular
Regulation Number: 870.2100
Classification Product Code: DPW
Date Received: 09/29/2008
Decision Date: 10/28/2008
Regulation Medical Specialty: Cardiovascular
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