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Advance Medical Designs, Inc. Sterile Ultrasound Gel

K163050 Class II Traditional
Decision Date
2017-10-25
Sponsor / Applicant
Advance Medical Designs, Inc.

Technical Specification

510(k) Submission ID K163050
Product Code MUI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1570
Decision Date 2017-10-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Advance Medical Designs, Inc. Sterile Ultrasound Gel received FDA 510(k) clearance under submission number K163050, sponsored by Advance Medical Designs, 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 2017-10-25.

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.