# Victus, Inc.

- Location (FDA's records): Miami, FL
- FDA decisions: 3 (2002–2010): 3 510(k) clearances
- Product codes: FPA (3)
- Predicates its devices cite: 20 (2 its own); citations of its devices by later devices: 3 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Icu Medical, Inc.: 6 (https://510kreport.com/company/icu-medical)
- Churchill Medical Systems, Inc.: 5 (https://510kreport.com/company/churchill-medical-systems)
- Mcgaw, Inc.: 3 (https://510kreport.com/company/mcgaw)
- Leventon, S.A.: 1 (https://510kreport.com/company/leventon)
- Hospira, Inc.: 1 (https://510kreport.com/company/hospira)
- Kendall Mcgaw Laboratories, Inc.: 1 (https://510kreport.com/company/kendall-mcgaw-laboratories)
- Amsino Intl., Inc.: 1 (https://510kreport.com/company/amsino-intl)

## Firms that cite its devices most
- Pentaferte S.P.A: 1 (https://510kreport.com/company/pentaferte)

## Its most-cited devices
- K023469: Victus I.V. Administration Set, Models 27058, 27059,27062 (2002), cited by 2
- K030246: Victus I.V. Administration Set, Models 27071 and 27072 (2003), cited by 1

## Recent decisions
- K093271: Extension Set (Standardbore Tubing), Extension Set (Minibore Tubing), IV Administration Set ( Standard (Jan 27, 2010)
- K030246: Victus I.V. Administration Set, Models 27071 and 27072 (Feb 26, 2003)
- K023469: Victus I.V. Administration Set, Models 27058, 27059,27062 (Dec 10, 2002)

Source page: https://510kreport.com/company/victus