FLUOBEAM LX Imaging System (FBLX); FLUOBEAM LM Imaging System (FBLM)— 510(k) K250455
Substantially EquivalentFluoptics Sas (A Getinge Group Company}
FDA 510(k) clearance K250455 for FLUOBEAM LX Imaging System (FBLX); FLUOBEAM LM Imaging System (FBLM), Substantially Equivalent on 2025-04-17. Applicant: Fluoptics Sas (A Getinge Group Company}.
Clearance details
- Applicant
- Fluoptics Sas (A Getinge Group Company}
- Product code
- Code QDG
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Grenoble, FR
Data sourced from openFDA. This site is unofficial and independent of the FDA.