Amydi-med Disposable Non-invasive EEG electrodes— 510(k) K240668
Substantially EquivalentShenzhen Amydi-Med Electrics Tech Co., Ltd.
FDA 510(k) clearance K240668 for Amydi-med Disposable Non-invasive EEG electrodes, Substantially Equivalent on 2024-03-19. Applicant: Shenzhen Amydi-Med Electrics Tech Co., Ltd.. Device class: 2.
Clearance details
- Applicant
- Shenzhen Amydi-Med Electrics Tech Co., Ltd.
- Product code
- Code GXY
- Device class
- Class 2
- Regulation
- 21 CFR 882.1320
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Shenzhen, CN
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Data sourced from openFDA. This site is unofficial and independent of the FDA.