Electrode Pad
FDA 510(k) clearance K241512 · decided 2025-01-15
Clearance details
- K-number
- K241512
- Device name
- Electrode Pad
- Applicant
- Shenzhen Deliduo Medical Technology Co.,Ltd
- Decision
- Substantially Equivalent
- Date received
- 2024-05-29
- Decision date
- 2025-01-15
- Days to decision
- 231 days
- Clearance type
- Traditional
- Product code
- GXY
- Device class
- 2
- Regulation number
- 882.1320
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- Huizhou, CN
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.