The following data is part of a premarket notification filed by Medrad, Inc. with the FDA for Medrad Envision Ct Injector And Qwik Fit Syringe.
| Device ID | K934086 |
| 510k Number | K934086 |
| Device Name: | MEDRAD ENVISION CT INJECTOR AND QWIK FIT SYRINGE |
| Classification | Injector And Syringe, Angiographic |
| Applicant | MEDRAD, INC. 271 KAPPA DR. Pittsburgh, PA 15238 -2870 |
| Contact | Jan E Burtick |
| Correspondent | Jan E Burtick 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 | 1993-08-24 |
| Decision Date | 1995-06-15 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00616258005485 | K934086 | 000 |