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Sonishield 100 Antimicrobial Ultrasound Gel

K151070 Class II Traditional
Decision Date
2016-01-13
Sponsor / Applicant
Quotient Medical

Technical Specification

510(k) Submission ID K151070
Product Code MUI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1570
Decision Date 2016-01-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Sonishield 100 Antimicrobial Ultrasound Gel received FDA 510(k) clearance under submission number K151070, sponsored by Quotient Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2016-01-13.

Classification & Regulation

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