AC Cream - Conductive paste

FDA 510(k) K212326 · Spes Medica Srl

Substantially Equivalent

510(k) numberK212326

Submission

Device name
AC Cream - Conductive paste
Applicant
Spes Medica Srl
Battipaglia, IT
Received
July 26, 2021
Decision date
December 1, 2021
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
GYB – Media, Electroconductive
Device class
Class II (moderate risk)
Regulation
21 CFR 882.1275
Specialty
Neurology

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K222770Conductive GelGYB · Traditional Top-Rank Health Care Co., Ltd.12/13/2022SE
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K212325EEG-acpGYB · Traditional Somnomedics GmbH06/15/2022SE
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K200402DR-HO'S Electro Therapy Conductive GelGYB · Traditional Guangzhou Xinbo Electronic Co., Ltd.11/25/2020SE
K191975Elefix V Paste for EEG & EMGGYB · Traditional Nihon Kohden Corporation02/07/2020SE
K192606SAC2 - Electrode CreamGYB · Traditional Spes Medica Srl01/17/2020SE
K190050Tech Dots - Adhesive and conductive gelGYB · Traditional Spes Medica Srl07/19/2019SE

More from Spes Medica Srl

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K211954Subdural Electrode, Strip/Intraoperative Strip, Grid/Intraoperative Grid, Multi-Strip…GYC · Traditional 11/10/2022SE
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K192603Spes Medica Subdermal Needle ElectrodesGXZ · Traditional 11/22/2019SE
K190050Tech Dots - Adhesive and conductive gelGYB · Traditional 07/19/2019SE
K133348Stim ProbeETN · Traditional 11/21/2014SE
K120494Disposable Adhesive Surface ElectrodeGXY · Traditional 06/11/2012SE
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Questions and answers

When was AC Cream - Conductive paste cleared by the FDA?

AC Cream - Conductive paste (K212326) received a 510(k) decision of Substantially Equivalent on December 1, 2021, 128 days after the submission was received.

What is the product code of K212326?

The FDA product code is GYB – Media, Electroconductive, a Class II (moderate risk) device regulated under 21 CFR 882.1275.