# K073094: VITALLINK3 Mobile Vital Signs System

- Pathway: 510(k) (Special)
- Applicant: Telemedic Systems, Ltd.
- Decided: Jan 4, 2008 after 64 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: 1 generation back to K010732 (2001). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K010732: Vitallink 1200 Mobile Vital Signs Systems (VL 1200 System), Telemedic Systems, Inc. (2001) Summary page 3.

## Indications for use
The VitalLink (VL3) Mobile Vital Signs System is intend for use as a portable vital signs monitor for patients who are remotely located from medical professionals. The system can be used to acquire and display vital signs from patients in remote locations and transmit the data, real time, to a medical professional at a Medical Call Center / Medical Service Provider in order to help determine the patient's transportation needs.

Source page: https://510kreport.com/device/K073094
Methodology: https://510kreport.com/methodology