K240964
- 510(k) number
- K240964
- Device name
- FLOW 90? Wand
- Applicant
- ArthroCare Corporation TX · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2024-05-08
- Date received
- 2024-04-09
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K240964.pdf
Official FDA record: K240964
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.