LEKSELL GAMMAPLAN— 510(k) K090972
Substantially EquivalentElekta Instrument AB
FDA 510(k) clearance K090972 for LEKSELL GAMMAPLAN, Substantially Equivalent on 2009-07-20. Applicant: Elekta Instrument AB.
Clearance details
- Applicant
- Elekta Instrument AB
- Product code
- Code MUJ
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Stockholm, SE
Data sourced from openFDA. This site is unofficial and independent of the FDA.