K233099
- 510(k) number
- K233099
- Device name
- Gladiator
- Applicant
- Rohrer Aesthetics, LLC AL · US
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2024-05-22
- Date received
- 2023-09-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K233099.pdf
Official FDA record: K233099
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.