The following data is part of a premarket notification filed by Sybron Corp. with the FDA for Digital Injector Sys.
| Device ID | K833138 |
| 510k Number | K833138 |
| Device Name: | DIGITAL INJECTOR SYS |
| Classification | Injector And Syringe, Angiographic |
| Applicant | SYBRON CORP. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | DXT |
| CFR Regulation Number | 870.1650 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-09-14 |
| Decision Date | 1983-11-14 |