The following data is part of a premarket notification filed by Centrix, Inc. with the FDA for Multi-purpose Dental Syringe.
| Device ID | K811831 |
| 510k Number | K811831 |
| Device Name: | MULTI-PURPOSE DENTAL SYRINGE |
| Classification | Syringe, Cartridge |
| Applicant | CENTRIX, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EJI |
| CFR Regulation Number | 872.6770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-06-29 |
| Decision Date | 1981-09-08 |