K232769
- 510(k) number
- K232769
- Device name
- BeaMed Laser Surgery Fibers
- Applicant
- Bt Beamedical Tachnoogies Ltd. (Beamed) IL
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2023-12-06
- Date received
- 2023-09-11
- 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: K232769.pdf
Official FDA record: K232769
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.