KONICA LD-4500 LASER DIGITIZER— 510(k) K933830
Substantially EquivalentKonica Medical Corp.
FDA 510(k) clearance K933830 for KONICA LD-4500 LASER DIGITIZER, Substantially Equivalent on 1993-12-14. Applicant: Konica Medical Corp..
Clearance details
- Applicant
- Konica Medical Corp.
- Product code
- Code LMA
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- New York, NY, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.