# K023120: Oxycon Mobile

- Pathway: 510(k) (Traditional)
- Applicant: Erich Jaeger GmbH
- Decided: Nov 12, 2003 after 419 days
- Product code: BZC (Calculator, Pulmonary Function Data)
- Device class: 2
- Regulation: 21 CFR 868.1880
- 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’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K162515: COSMED K5 Wearable Metabolic Technology (2017), 0 descendants of its own

## Indications for use
The Jaeger OXYCON MOBILE pulmonary function mobile test system is a device which monitors the cardio-respiratory functions during stress testing, rehabilitation, sports medicine and other related activities. The OXYCON MOBILE system allows the use of telemetry for the monitoring of metabolic parameters, The OXYCON MOBILE system is intended to use with adults and children over the age of 14 years.

Source page: https://510kreport.com/device/K023120
Methodology: https://510kreport.com/methodology