Conductivity Gel
FDA 510(k) K871913 · Futuremed Div. of Future Impex Corp.
510(k) numberK871913
Submission
- Device name
- Conductivity Gel
- Applicant
- Futuremed Div. of Future Impex Corp.
Deerpark, NY, US - Received
- May 18, 1987
- Decision date
- July 15, 1987
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
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|---|---|---|---|
| K243749 | Jmoon Conductive GelGYB · Traditional | Shenzhen Ulike Smart Electronics Co., Ltd. | 04/08/2025SE |
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| K222770 | Conductive GelGYB · Traditional | Top-Rank Health Care Co., Ltd. | 12/13/2022SE |
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| K200402 | DR-HO'S Electro Therapy Conductive GelGYB · Traditional | Guangzhou Xinbo Electronic Co., Ltd. | 11/25/2020SE |
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| K871421 | Model HL-100 Portable DC Elect. Therapeutic UnitIPF · Traditional | 01/22/1988SE |
| K873817 | Spiro Analyzer ST-300BZG · Traditional | 12/02/1987SE |
| K872044 | Carbon ElectrodeGXY · Traditional | 07/16/1987SE |
| K872045 | Conductivity GelGYB · Traditional | 07/15/1987SE |
Questions and answers
When was Conductivity Gel cleared by the FDA?
Conductivity Gel (K871913) received a 510(k) decision of Substantially Equivalent on July 15, 1987, 58 days after the submission was received.
What is the product code of K871913?
The FDA product code is GYB – Media, Electroconductive, a Class II (moderate risk) device regulated under 21 CFR 882.1275.