K243682
- 510(k) number
- K243682
- Device name
- SonoPlex STIM; SonoPlex II
- Applicant
- PAJUNK GmbH Medizintechnologie DE
- Product code
- BSP — Needle, Conduction, Anesthetic (W/Wo Introducer)
- Decision date
- 2025-06-27
- Date received
- 2024-11-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K243682.pdf
Official FDA record: K243682
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.