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SOUND IMAGER I

K833231 Class II Traditional
Decision Date
1984-02-04
Sponsor / Applicant
Sound Imaging, Inc.

Technical Specification

510(k) Submission ID K833231
Product Code IYO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1560
Decision Date 1984-02-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SOUND IMAGER I received FDA 510(k) clearance under submission number K833231, sponsored by Sound Imaging, 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 1984-02-04.

Classification & Regulation

This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.