# K033133: Telecare D.R. Server Software System

- Pathway: 510(k) (Traditional)
- Applicant: Healthcare Vision, Inc.
- Decided: Apr 13, 2004 after 196 days
- Product code: MWI (Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms))
- Device class: 2
- Regulation: 21 CFR 870.2300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K981533 (1998). 5 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K020584: N2000 Base Station; N2001 Nurse Station, Neptec Design Group, Ltd. (2002) Summary page 3.
- K001308: Modification to Zymed Telemetry System, Model Easiview, Agilent Technologies (2000) Summary page 3.

## Most influential descendants
- K073710: Intouch Remote Presence Robotic System, Model RP-7 (2008), 2 descendants of its own
- K120895: Remote Presence System (2012), 1 descendant of its own
- K123229: Remote Presence System, Model RP-Vita (2012), 0 descendants of its own

## Indications for use
The Telecare®D.R. is intended to be used in conjunction with 510(k) certified devices that upon prescription by an authorized healthcare provider for patients provides a means of receiving and storing audio, video, and patient biometric data including vital signs information received over standard phone lines or high speed connection between patients, typically at home, and health professionals at the health care provider's site.

Source page: https://510kreport.com/device/K033133
Methodology: https://510kreport.com/methodology