The following data is part of a premarket notification filed by E.c. Moore Co. with the FDA for Howmedica Brass Center Disc.
| Device ID | K790640 |
| 510k Number | K790640 |
| Device Name: | HOWMEDICA BRASS CENTER DISC |
| Classification | Disk, Abrasive |
| Applicant | E.C. MOORE CO. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | EHJ |
| CFR Regulation Number | 872.6010 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1979-03-30 |
| Decision Date | 1979-05-01 |