The following data is part of a premarket notification filed by Travenol Laboratories, S.a. with the FDA for A.v. Fistula Cannulation Sets.
| Device ID | K830021 |
| 510k Number | K830021 |
| Device Name: | A.V. FISTULA CANNULATION SETS |
| Classification | Accessories, Blood Circuit, Hemodialysis |
| Applicant | TRAVENOL LABORATORIES, S.A. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | KOC |
| CFR Regulation Number | 876.5820 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-01-04 |
| Decision Date | 1983-01-14 |