# K072590: Inspiration; Ventilator System, LS Ventilator System, Infant Ventilator System and Infant LS Ventilator System

- Pathway: 510(k) (Traditional)
- Applicant: Event Medical, Inc.
- Decided: Jan 4, 2008 after 112 days
- Product code: CBK (Ventilator, Continuous, Facility Use)
- Device class: 2
- Regulation: 21 CFR 868.5895
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 7 generations back to K902859 (1991). 30 ancestors in all.
2 later devices descend from it; 2 cite it directly.
3 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051550: Inspiration Ventilator System, eVent Medical, Ltd. (2005) Summary page 1.
- K062093: Avea Ventilator, Viasys Respiratory Care, Inc. (2006) Summary page 1.

## Most influential descendants
- K130178: Inspiration Ventilator System 5I/7I (2013), 0 descendants of its own
- K113743: Evolution 3E Ventilator (2012), 0 descendants of its own

## Indications for use
The Inspiration® Ventilator is indicated for use with a wide range of patients from infant through adult, requiring respiratory support for a wide range of clinical conditions in hospital, hospital-type facilities and intra-hospital transport.

Source page: https://510kreport.com/device/K072590
Methodology: https://510kreport.com/methodology