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NODECREST TRANSCRANICAL DOPPLER ULTRASOUND SYSTEM

K060112 Class II Traditional
Decision Date
2006-05-05
Sponsor / Applicant
Nodecrest, LLC

Technical Specification

510(k) Submission ID K060112
Product Code IYN
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1550
Decision Date 2006-05-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NODECREST TRANSCRANICAL DOPPLER ULTRASOUND SYSTEM received FDA 510(k) clearance under submission number K060112, sponsored by Nodecrest, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2006-05-05.

Classification & Regulation

This clearance is catalogued under FDA product code IYN and 21 CFR 892.1550, within the Radiology review panel as a Class II device.