K252592
- 510(k) number
- K252592
- Device name
- TELLTALE Electrosurgical Guidewire System
- Applicant
- Telltale, LLC MA · US
- Product code
- SGO — Percutaneous Catheter For Electrosurgical Cutting He
- Decision date
- 2025-11-13
- Date received
- 2025-08-15
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K252592.pdf
Official FDA record: K252592
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.