# K890606: Ohmeda 5330 Agent Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Ohmeda Medical
- Decided: Apr 20, 1989 after 73 days
- Product code: CBQ (Analyzer, Gas, Enflurane, Gaseous-Phase (Anesthetic Concentration))
- Device class: 2
- Regulation: 21 CFR 868.1500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K962648: Ohmeda Model 5330 Anesthetic Agent Monitor (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K890606
Methodology: https://510kreport.com/methodology