The following data is part of a premarket notification filed by Multi Media Dental Systems, Inc. with the FDA for Mediadent Hdx/mmd Hdx Sp Xray Sensor.
| Device ID | K002425 |
| 510k Number | K002425 |
| Device Name: | MEDIADENT HDX/MMD HDX SP XRAY SENSOR |
| Classification | System, X-ray, Extraoral Source, Digital |
| Applicant | MULTI MEDIA DENTAL SYSTEMS, INC. 1302 MACY DR. Roswell, GA 30076 |
| Contact | Scott Mclaughlin |
| Correspondent | Scott Mclaughlin MULTI MEDIA DENTAL SYSTEMS, INC. 1302 MACY DR. Roswell, GA 30076 |
| Product Code | MUH |
| CFR Regulation Number | 872.1800 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-08-08 |
| Decision Date | 2000-12-21 |