The following data is part of a premarket notification filed by Cook Incorporated with the FDA for Transjugular Liver Access Sets.
| Device ID | K171820 |
| 510k Number | K171820 |
| Device Name: | Transjugular Liver Access Sets |
| Classification | Introducer, Catheter |
| Applicant | Cook Incorporated 750 Daniels Way Bloomington, IN 47404 |
| Contact | David Lehr |
| Correspondent | David Lehr Cook Incorporated 750 Daniels Way Bloomington, IN 47404 |
| Product Code | DYB |
| CFR Regulation Number | 870.1340 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-06-19 |
| Decision Date | 2018-03-09 |
| Summary: | summary |