The following data is part of a premarket notification filed by Canon Inc. with the FDA for Digital Radiography Cxdi-50c.
| Device ID | K060433 |
| 510k Number | K060433 |
| Device Name: | DIGITAL RADIOGRAPHY CXDI-50C |
| Classification | Solid State X-ray Imager (flat Panel/digital Imager) |
| Applicant | CANON INC. ONE CANON PLAZA Lake Success, NY 11042 |
| Contact | Sheila Driscoll |
| Product Code | MQB |
| CFR Regulation Number | 892.1680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2006-02-21 |
| Decision Date | 2006-03-10 |
| Summary: | summary |