# K123868: Interlink System Lever Lock Cannula with Check Valve, Secondary Medication Sets, Solution Sets, Continu-Flo Solution Set

- Pathway: 510(k) (Special)
- Applicant: Baxter Healthcare Corp
- Decided: Jan 8, 2013 after 22 days
- Product code: FPA (Set, Administration, Intravascular)
- Device class: 2
- Regulation: 21 CFR 880.5440
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K883638 (1988). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K883638: Safesite Injection Site and Blunt Cannula, Baxter Healthcare Corp (1988) Summary page 2.

## Indications for use
For the administration of fluids from a container to the patient through a vascular access device. The Interlink Lever Lack Cannula is indicated to function exclusively with the Interlink Injection Site as a fluid path injection device.

Source page: https://510kreport.com/device/K123868
Methodology: https://510kreport.com/methodology