# K010732: Vitallink 1200 Mobile Vital Signs Systems (VL 1200 System)

- Pathway: 510(k) (Traditional)
- Applicant: Telemedic Systems, Inc.
- Decided: Sep 27, 2001 after 199 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
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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K073094: VITALLINK3 Mobile Vital Signs System (2008), 0 descendants of its own

Source page: https://510kreport.com/device/K010732
Methodology: https://510kreport.com/methodology