# P210018: Et Control

- Pathway: PMA
- Applicant: Datex-Ohmeda, Inc., A General Electric Company
- Decided: Mar 17, 2022 after 318 days
- Product code: QSF (Software Option For Anesthesia Gas Machine To Achieve And Maintain Targeted End Tidal Oxygen And Anesthetic Agents)
- Device class: 3
- Recalls of this device: 1 (1 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
1 of 1 device in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. PMA decisions do not claim a predicate device.

## Recalls of this device
- Jul 12, 2024 · Class I · Z-0083-2025: Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.

Source page: https://510kreport.com/device/P210018
Methodology: https://510kreport.com/methodology