# K092382: Nexus Pressure Rated Extension Sets

- Pathway: 510(k) (Traditional)
- Applicant: Nexus Medical, LLC
- Decided: Apr 26, 2010 after 264 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
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K181895: Kurin PIV Blood Collection Set with High Pressure (2019), 0 descendants of its own

## Indications for use
The Nexus Pressure Rated Extension Sets are intended for use in today's growing professional healthcare environment, including healthcare facilities that utilize infusion systems to administer IV fluids, medications, blood and blood products to the patient's vascular system and may be safely used with power injectors at pressures up to 325 psi. The needle-free design allows the user to add medication into the primary line and may also aid in the prevention of needle stick injuries.

Source page: https://510kreport.com/device/K092382
Methodology: https://510kreport.com/methodology