KONICA LASER IMAGER, MODEL DRYPRO MODEL 771— 510(k) K032681
Substantially EquivalentKonica Medical and Graphic Corporation
FDA 510(k) clearance K032681 for KONICA LASER IMAGER, MODEL DRYPRO MODEL 771, Substantially Equivalent on 2003-09-24. Applicant: Konica Medical and Graphic Corporation.
Clearance details
- Applicant
- Konica Medical and Graphic Corporation
- Product code
- Code LMC
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Mie-Ken, JP
Data sourced from openFDA. This site is unofficial and independent of the FDA.