K251899
- 510(k) number
- K251899
- Device name
- E Blator
- Applicant
- New Deantronics Taiwan , Ltd. TW
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2025-10-01
- Date received
- 2025-06-20
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K251899.pdf
Official FDA record: K251899
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.