The following data is part of a premarket notification filed by Medtec, Inc. with the FDA for Med-tec, Inc. Breast Board, Mt-200.
| Device ID | K935412 |
| 510k Number | K935412 |
| Device Name: | MED-TEC, INC. BREAST BOARD, MT-200 |
| Classification | Accelerator, Linear, Medical |
| Applicant | MEDTEC, INC. 1401 8TH ST. S.E. P.O. BOX 602 Orange City, IA 51041 |
| Contact | Donald Riibe |
| Correspondent | Donald Riibe MEDTEC, INC. 1401 8TH ST. S.E. P.O. BOX 602 Orange City, IA 51041 |
| Product Code | IYE |
| CFR Regulation Number | 892.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-11-09 |
| Decision Date | 1994-07-18 |