The following data is part of a premarket notification filed by Dyna-med with the FDA for Bite Stick, Dyna.
| Device ID | K760258 |
| 510k Number | K760258 |
| Device Name: | BITE STICK, DYNA |
| Classification | Block, Bite |
| Applicant | DYNA-MED 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | JXL |
| CFR Regulation Number | 882.5070 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-07-20 |
| Decision Date | 1976-07-26 |