The following data is part of a premarket notification filed by Medrad, Inc. with the FDA for Medrad Varible Infusion Injector.
| Device ID | K905819 |
| 510k Number | K905819 |
| Device Name: | MEDRAD VARIBLE INFUSION INJECTOR |
| Classification | Injector And Syringe, Angiographic |
| Applicant | MEDRAD, INC. 271 KAPPA DR. Pittsburgh, PA 15238 -2870 |
| Contact | Francis X Dobscha |
| Correspondent | Francis X Dobscha MEDRAD, INC. 271 KAPPA DR. Pittsburgh, PA 15238 -2870 |
| Product Code | DXT |
| CFR Regulation Number | 870.1650 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1990-12-31 |
| Decision Date | 1991-09-16 |