The following data is part of a premarket notification filed by Coeur, Inc. with the FDA for Adapters For Ct, Angiographic, And/or Mri Power Injectors.
| Device ID | K070798 |
| 510k Number | K070798 |
| Device Name: | ADAPTERS FOR CT, ANGIOGRAPHIC, AND/OR MRI POWER INJECTORS |
| Classification | Injector And Syringe, Angiographic |
| Applicant | COEUR, INC. 704 CADET COURT Lebanon, TN 37087 |
| Contact | Debra F Manning |
| Correspondent | Debra F Manning COEUR, INC. 704 CADET COURT Lebanon, TN 37087 |
| Product Code | DXT |
| CFR Regulation Number | 870.1650 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-03-23 |
| Decision Date | 2007-10-04 |
| Summary: | summary |