Konica Medical and Graphic Corporation · Class II · Cleared Sep 24, 2003
| K-number | K032681 |
| Device name | KONICA LASER IMAGER, MODEL DRYPRO MODEL 771 |
| Applicant | Konica Medical and Graphic Corporation |
| Product code | LMC |
| Device class | Class II |
| Decision date | Sep 24, 2003 |
| Decision | Substantially Equivalent |
| Regulation | 892.2040 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov