The following data is part of a premarket notification filed by Siemens Medical Laboratories, Inc. with the FDA for Mevatron 67e.
| Device ID | K812032 |
| 510k Number | K812032 |
| Device Name: | MEVATRON 67E |
| Classification | Accelerator, Linear, Medical |
| Applicant | SIEMENS MEDICAL LABORATORIES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | IYE |
| CFR Regulation Number | 892.5050 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-07-20 |
| Decision Date | 1981-08-18 |