The following data is part of a premarket notification filed by Fred M. Davis with the FDA for The Toothpik.
| Device ID | K830225 |
| 510k Number | K830225 |
| Device Name: | THE TOOTHPIK |
| Classification | Floss, Dental |
| Applicant | FRED M. DAVIS 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | JES |
| CFR Regulation Number | 872.6390 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-01-24 |
| Decision Date | 1983-02-18 |