# K093134: Cerner Careaware Ibus

- Pathway: 510(k) (Traditional)
- Applicant: Cerner Corp.
- Decided: Nov 27, 2009 after 53 days
- Product code: DRG (Transmitters And Receivers, Physiological Signal, Radiofrequency)
- Device class: 2
- Regulation: 21 CFR 870.2910
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
7 later devices descend from it; 1 cites it directly.
0 of 8 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
- K100133: Airstrip Remote Patient Monitoring (RPM) Remote Data Viewing Software, Version 3.1 (2010), 6 descendants of its own
- K142106: Decisio Health Patient Dashboard (2015), 5 descendants of its own
- K213335: Capsule Surveillance System (2022), 3 descendants of its own
- K241958: WARD-CSS (v1.2.x) (2025), 0 descendants of its own
- K240756: Aitrics-VC (2024), 0 descendants of its own

## Indications for use
Cerner iBus is a software application intended for use in the transportation, aggregation and derivation of data between medical devices and external systems used in a clinical setting for the purpose of automating data collection and clinical information management. Cerner iBus is not intended to directly monitor, diagnose or treat patients or to be used in the prevention of a disease or condition, nor does Cerner iBus come into direct contact with patients.

Source page: https://510kreport.com/device/K093134
Methodology: https://510kreport.com/methodology