The following data is part of a premarket notification filed by Canon, Inc. with the FDA for Digital Radiography Cxdi-401c Wireless.
| Device ID | K133693 |
| 510k Number | K133693 |
| Device Name: | DIGITAL RADIOGRAPHY CXDI-401C WIRELESS |
| Classification | Solid State X-ray Imager (flat Panel/digital Imager) |
| Applicant | CANON, INC. 1201 RICHARDSON DRIVE, STE 280 Richardson, TX 75080 |
| Contact | Diane Rutherford |
| Correspondent | Diane Rutherford CANON, INC. 1201 RICHARDSON DRIVE, STE 280 Richardson, TX 75080 |
| Product Code | MQB |
| CFR Regulation Number | 892.1680 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-12-03 |
| Decision Date | 2014-07-01 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04960999999043 | K133693 | 000 |