The following data is part of a premarket notification filed by Septodont, Inc. with the FDA for Racestyptine Cord.
| Device ID | K760657 |
| 510k Number | K760657 |
| Device Name: | RACESTYPTINE CORD |
| Classification | Retractor, All Types |
| Applicant | SEPTODONT, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
| Product Code | EIG |
| CFR Regulation Number | 872.4565 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1976-09-15 |
| Decision Date | 1976-09-27 |