Advance Medical Designs, Inc. Sterile Ultrasound Gel

FDA 510(k) K163050 · Advance Medical Designs, Inc.

Substantially Equivalent

510(k) numberK163050

Submission

Device name
Advance Medical Designs, Inc. Sterile Ultrasound Gel
Applicant
Advance Medical Designs, Inc.
Marietta, GA, US
Received
November 1, 2016
Decision date
October 25, 2017
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MUI – Media, Coupling, Ultrasound
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1570
Specialty
Radiology

Other 510(k)s with product code MUI

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K253255Non-Sterile Ultrasound Gel Sterile Ultrasound GelMUI · Traditional Foshan Pingchuang Medical Technology Co., Ltd.06/17/2026SE
K252337EdgeFlow Gel PadMUI · Traditional Edgecare, Inc.04/24/2026SE
K242167Sterile and Non-Sterile Ultrasonic Coupling AgentMUI · Traditional Anhui Deepblue Medical Technology Co., Ltd.09/19/2024SE
K241789Non-Sterile Ultrasound Transmission GelsMUI · Traditional Hony Medical Co., Ltd.07/24/2024SE
K232957Sterile and Non-Sterile Ultrasound GelsMUI · Traditional Jianerkang Medical Co., Ltd.12/15/2023SE
K221999Ultrasound Transmission GelsMUI · Traditional Hony Medical Co., Ltd.08/30/2022SE
K211691Ultrast GelMUI · Traditional Ultrast, Inc.12/22/2021SE
K190591Safergel Sterile Ultrasound GelMUI · Traditional Safersonic Us, Inc.10/04/2019SE
K181363EcoVue Sterile and Non-Sterile Ultrasound GelsMUI · Traditional H R Pharmaceuticals, Inc.06/13/2018SE
K163027Ultra/Phonic Free Conductivity GelMUI · Traditional Pharmaceutical Innovations, Inc.01/09/2018SE

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Questions and answers

When was Advance Medical Designs, Inc. Sterile Ultrasound Gel cleared by the FDA?

Advance Medical Designs, Inc. Sterile Ultrasound Gel (K163050) received a 510(k) decision of Substantially Equivalent on October 25, 2017, 358 days after the submission was received.

What is the product code of K163050?

The FDA product code is MUI – Media, Coupling, Ultrasound, a Class II (moderate risk) device regulated under 21 CFR 892.1570.