# K071301: Antlia I Wound Irrigation System

- Pathway: 510(k) (Traditional)
- Applicant: Innovative Therapies, Inc.
- Decided: May 24, 2007 after 15 days
- Product code: OMP (Negative Pressure Wound Therapy Powered Suction Pump)
- Device class: 2
- Regulation: 21 CFR 878.4780
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K945062 (1995). 4 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K021501: V.a.C. Instillamat (Vacuum Assisted Closure Instillamat, Kinetic Concepts, Inc. (2002) Summary page 1.

## Most influential descendants
- K093564: Sved Wound Treatment System (2009), 2 descendants of its own
- K142916: SVED Wound Treatment System (2015), 1 descendant of its own
- K231646: Carilex VT¿200-i NX (2024), 0 descendants of its own

## Indications for use
The ANTLIA I™ Wound Irrigation System device is indicated for patients who would benefit from vacuum assisted drainage and controlled delivery of topical wound treatment solutions and suspensions over the wound bed. The ANTLIA I™ Wound Irrigation System is intended for patients with chronic, acute, traumatic, subacute, and dehisced wounds, diabetic ulcers, pressure ulcers, flaps and grafts.

Source page: https://510kreport.com/device/K071301
Methodology: https://510kreport.com/methodology