# K171029: eCareCoordinator

- Pathway: 510(k) (Traditional)
- Applicant: Visicu, Inc.
- Decided: Jul 14, 2017 after 99 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
Longest line of descent: 6 generations back to K864318 (1987). 19 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 21 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K141706: Ecare Coordinator (Ecc), Visicu, Inc. (2014) Summary page 4.

## Most influential descendants
- K222398: Care Team Portal (2023), 0 descendants of its own

## Indications for use
eCareCoordinator and its accessories are indicated for use by patients and by care teams for collecting and reviewing patient data from patients who are capable and willing to engage in use of this software, to transmit medical and non-medical information through integrated technologies.

Source page: https://510kreport.com/device/K171029
Methodology: https://510kreport.com/methodology