K242207
- 510(k) number
- K242207
- Device name
- NOABLE LASER
- Applicant
- Daeju Meditech Engineering Co., Ltd. KR
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2025-03-07
- Date received
- 2024-07-29
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K242207.pdf
Official FDA record: K242207
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.