The following data is part of a premarket notification filed by Midwest with the FDA for Mw-8000.
| Device ID | K792304 |
| 510k Number | K792304 |
| Device Name: | MW-8000 |
| Classification | Handpiece, Air-powered, Dental |
| Applicant | MIDWEST 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EFB |
| CFR Regulation Number | 872.4200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-11-16 |
| Decision Date | 1979-11-27 |