# K844433: Vaccess 2000 Single Lumen Subclavian Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Vas-Cath of Canada, Ltd.
- Decided: Mar 13, 1985 after 117 days
- Product code: LFJ (Catheter, Subclavian)
- Device class: 2
- Regulation: 21 CFR 876.5540
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Recalls of this device
- Aug 10, 2007 · Not classified · Z-1229-2007: Metal guidewires used in Hemodialysis Catheters may have been reverse loaded within the dispenser. Potential exists for the stiff end of the guidewire to be inserted into the patient instead of the fl

Source page: https://510kreport.com/device/K844433
Methodology: https://510kreport.com/methodology