meddevicedb.com FDA Device Reference

Touch Ultrasound

K150342 Class II Traditional
Decision Date
2015-05-08
Sponsor / Applicant
Carestream Health, Inc.

Technical Specification

510(k) Submission ID K150342
Product Code IYO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1560
Decision Date 2015-05-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Touch Ultrasound received FDA 510(k) clearance under submission number K150342, sponsored by Carestream Health, 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 2015-05-08.

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.