The following data is part of a premarket notification filed by Vas-cath Of Canada Ltd. with the FDA for Parallel Dual Lumen Subclavian Cannula.
| Device ID | K834358 |
| 510k Number | K834358 |
| Device Name: | PARALLEL DUAL LUMEN SUBCLAVIAN CANNULA |
| Classification | Cannula, A-v Shunt |
| Applicant | VAS-CATH OF CANADA LTD. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | FIQ |
| CFR Regulation Number | 876.5540 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1983-12-13 |
| Decision Date | 1984-04-02 |