# K023469: Victus I.V. Administration Set, Models 27058, 27059,27062

- Pathway: 510(k) (Traditional)
- Applicant: Victus, Inc.
- Decided: Dec 10, 2002 after 55 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 K921860 (1992). 1 ancestor in all.
2 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K921860: Modification to IV Spike, Mcgaw, Inc. (1992) Summary page 1.
- (no number) BBraun-McGaw N Administration Sets (pre-Amendment): named in the summary without a submission number

## Cited in the summary but kept off the family tree
- K093265: BBraun-McGaw N Administration Sets. Not in FDA’s 510(k), De Novo or PMA lists as we hold them (a misreading, a typo, or a number FDA does not list), so it is kept off the family tree

## Most influential descendants
- K093271: Extension Set (Standardbore Tubing), Extension Set (Minibore Tubing), IV Administration Set ( Standard (2010), 0 descendants of its own
- K041495: Pentadeflue IV Solution Administration Sets (2005), 0 descendants of its own

## Indications for use
To administer IV fluid/medication to the patient’s vascular system.

Source page: https://510kreport.com/device/K023469
Methodology: https://510kreport.com/methodology