K231948
- 510(k) number
- K231948
- Device name
- MEDIYAG
- Applicant
- Medicreations, LLC NV · US
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2024-10-09
- Date received
- 2023-06-30
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K231948.pdf
Official FDA record: K231948
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.