K242286
- 510(k) number
- K242286
- Device name
- Superflow Prime Treatment System (ASP-1M)
- Applicant
- Guangzhou Aimira Innovation Technology Co, Ltd. CN
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2024-11-08
- Date received
- 2024-08-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K242286.pdf
Official FDA record: K242286
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.