K242841
- 510(k) number
- K242841
- Device name
- Disposable RF Electrode (RFDE-5/RFDE-10/RFDE-15/RFDE-20)
- Applicant
- ABBOTT MEDICAL TX · US
- Product code
- GXI — Probe, Radiofrequency Lesion
- Decision date
- 2025-05-27
- Date received
- 2024-09-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
510(k) Summary (official FDA PDF): K242841.pdf
Official FDA record: K242841
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.