The following data is part of a premarket notification filed by Cordis Corp. with the FDA for Cordis Endeavor.
| Device ID | K970842 |
| 510k Number | K970842 |
| Device Name: | CORDIS ENDEAVOR |
| Classification | Catheter, Continuous Flush |
| Applicant | CORDIS CORP. 14201 N.W. 60TH AVE. Miami Lakes, FL 33014 |
| Contact | Tamara Yount |
| Correspondent | Tamara Yount CORDIS CORP. 14201 N.W. 60TH AVE. Miami Lakes, FL 33014 |
| Product Code | KRA |
| CFR Regulation Number | 870.1210 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-03-07 |
| Decision Date | 1997-05-28 |
| Summary: | summary |