K232568
- 510(k) number
- K232568
- Device name
- IPG Medical Family of Thulium Fiber Lasers, Surgical Fibers, and Accessories
- Applicant
- Ipg Medical Corporation MA · US
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2024-03-21
- Date received
- 2023-08-24
- 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: K232568.pdf
Official FDA record: K232568
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.