meddevicedb.com FDA Device Reference

SONICEYE ULTRASOUND TRANSDUCER

K113832 Class II Abbreviated
Decision Date
2012-03-06
Sponsor / Applicant
Blacktoe Medical Iii, Inc.

Technical Specification

510(k) Submission ID K113832
Product Code ITX
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1570
Decision Date 2012-03-06
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SONICEYE ULTRASOUND TRANSDUCER received FDA 510(k) clearance under submission number K113832, sponsored by Blacktoe Medical Iii, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2012-03-06.

Classification & Regulation

This clearance is catalogued under FDA product code ITX and 21 CFR 892.1570, within the Radiology review panel as a Class II device.