# K030246: Victus I.V. Administration Set, Models 27071 and 27072

- Pathway: 510(k) (Traditional)
- Applicant: Victus, Inc.
- Decided: Feb 26, 2003 after 33 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). 5 ancestors in all.
1 later device descends from it; 1 cites it directly.
1 of 7 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K921860: Modification to IV Spike, Mcgaw, Inc. (1992) Summary page 1.
- K964435: Primary IV Set, Icu Medical, Inc. (1997) Summary page 1.
- K915571: Clave Connector, Icu Medical, Inc. (1992) Summary page 1.
- K941190: Clave Needle-Less Connector Open Extension Set, Icu Medical, Inc. (1995) Summary page 1.
- K970855: Clave Connector, Icu Medical, Inc. (1997) Summary page 1.

## Cited in the summary but kept off the family tree
- K093265: BBraudMcGaw IV 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

## Indications for use
To administer IV fluiddmedication to the patient's vascular system through a needle-free system that aids in the elimination of needle-stick injury.

Source page: https://510kreport.com/device/K030246
Methodology: https://510kreport.com/methodology