# K080695: Mobile I.V. Systems 10,20,60

- Pathway: 510(k) (Abbreviated)
- Applicant: Northwind Technologies, Corp.
- Decided: Jul 1, 2008 after 112 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 K061115 (2006). 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)
- K061115: Speedflow 0.2UM Filter, Model 11214; Speedflow 1.2UM Filter,  Model 11215; Easydrop Controller, Model 11216, Gvs Spa (2006) Summary page 1.

## Indications for use
Indicated as a single use, sterile device for use in I.V. therapy when an extended fluid path is required for administration.

Source page: https://510kreport.com/device/K080695
Methodology: https://510kreport.com/methodology