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DIAGNOSTIC ULTRASOUND, MODEL 1.0

K992378 Class II Traditional
Decision Date
1999-09-29
Sponsor / Applicant
Volumetrics Medical Imaging, Inc.

Technical Specification

510(k) Submission ID K992378
Product Code IYO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1560
Decision Date 1999-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIAGNOSTIC ULTRASOUND, MODEL 1.0 received FDA 510(k) clearance under submission number K992378, sponsored by Volumetrics Medical 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 1999-09-29.

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.