# K920061: Hemometrix Continuous Blood Gas Monitoring System

- Pathway: 510(k) (Traditional)
- Applicant: Abbott Laboratories
- Decided: Mar 30, 1992 after 83 days
- Product code: CBZ (Analyzer, Ion, Hydrogen-Ion (Ph), Blood-Phase, Indwelling)
- Device class: 2
- Regulation: 21 CFR 868.1170
- Recalls of this device: none
- 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.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

Source page: https://510kreport.com/device/K920061
Methodology: https://510kreport.com/methodology