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FDA 510(k), K060112, NODECREST TRANSCRANICAL DOPPLER ULTRASOUND SYSTEM
FDA 510(k), K060112, NODECREST TRANSCRANICAL DOPPLER ULTRASOUND SYSTEM
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510(K) Number: K060112
Device Name: NODECREST TRANSCRANICAL DOPPLER ULTRASOUND SYSTEM
Manufacturer: NODECREST LLC
Device Classification Name: system, imaging, pulsed doppler, ultrasonic
Regulation Number: 892.1550
Classification Product Code: IYN
Date Received: 01/17/2006
Decision Date: 05/05/2006
Regulation Medical Specialty: Radiology
Device Name: NODECREST TRANSCRANICAL DOPPLER ULTRASOUND SYSTEM
Manufacturer: NODECREST LLC
Device Classification Name: system, imaging, pulsed doppler, ultrasonic
Regulation Number: 892.1550
Classification Product Code: IYN
Date Received: 01/17/2006
Decision Date: 05/05/2006
Regulation Medical Specialty: Radiology
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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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