# K092263: Enduravent-5 Ventilator

- Pathway: 510(k) (Traditional)
- Applicant: Providence Global Medical, Inc.
- Decided: Jan 21, 2010 after 177 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: 1 generation back to K002951 (2000). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K002951: Magellan Ventilator, Oceanic Medical Products, Inc. (2000) Summary page 1.

## Indications for use
EnduraVent-5 Ventilator is indicated to provide mechanical ventilation for adults and pediatric patients (pediatrics greater than 9 kg body weight) during in-hospital transport only

Source page: https://510kreport.com/device/K092263
Methodology: https://510kreport.com/methodology