# K092864: Aespire 7900, Aespire View

- Pathway: 510(k) (Special)
- Applicant: Datex-Ohmeda Inc., A Division of Instrumentarium C
- Decided: Jan 12, 2010 after 117 days
- Product code: BSZ (Gas-Machine, Anesthesia)
- Device class: 2
- Regulation: 21 CFR 868.5160
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K930017 (1994). 15 ancestors in all.
3 later devices descend from it; 1 cites it directly.
3 of 19 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050626: GE Datex-Ohmeda Aespire 7900 Anesthesia System, Datex-Ohmeda, Inc. (2005) Summary page 2.
- K090233: GE Datex-Ohmeda Aisys, Datex-Ohmeda, Inc. (2009) Summary page 2.

## Most influential descendants
- K122445: Aespire 7900, Aespire View (2012), 2 descendants of its own
- K143530: Aespire View (2015), 1 descendant of its own
- K172045: Aestiva 7900, Aestiva MRI, Aestiva 7100, Aestiva 7100 Compact, Aespire 100, Aespire 7100, Aespire 7900, Aespire View, Avance, Avance CS2, Aisys, Aisys CS2 (2017), 0 descendants of its own

## Indications for use
The family of GE Datex-Ohmeda Aespire anesthesia systems with 7900 ventilator (Aespire 7900 and Aespire View) is intended to provide general inhalation anesthesia and ventilatory support to a wide range of patients. The devices are intended for volume or pressure control ventilation. The devices are not suitable for use in a MRI environment.

Source page: https://510kreport.com/device/K092864
Methodology: https://510kreport.com/methodology