The following data is part of a premarket notification filed by Centrix, Inc. with the FDA for Pre-loaded C-r Tubes For Syringe.
| Device ID | K833725 |
| 510k Number | K833725 |
| Device Name: | PRE-LOADED C-R TUBES FOR SYRINGE |
| Classification | Material, Tooth Shade, Resin |
| Applicant | CENTRIX, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | EBF |
| CFR Regulation Number | 872.3690 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-10-24 |
| Decision Date | 1984-03-30 |