meddevicedb.com FDA Device Reference

HD-IVUS ULTRASOUND IMAGING SYSTEM

K112997 Class II Traditional
Decision Date
2011-12-17
Sponsor / Applicant
Silicon Vally Medical Instruments, Inc.

Technical Specification

510(k) Submission ID K112997
Product Code IYN
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1550
Decision Date 2011-12-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HD-IVUS ULTRASOUND IMAGING SYSTEM received FDA 510(k) clearance under submission number K112997, sponsored by Silicon Vally Medical Instruments, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2011-12-17.

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.