Fluobeam LX— 510(k) K190891
Substantially EquivalentFluoptics
FDA 510(k) clearance K190891 for Fluobeam LX, Substantially Equivalent on 2019-07-31. Applicant: Fluoptics.
Clearance details
- Applicant
- Fluoptics
- Product code
- Code QDG
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Grenoble Cedex 9, FR
Data sourced from openFDA. This site is unofficial and independent of the FDA.