# K052751: Ventlink System

- Pathway: 510(k) (Traditional)
- Applicant: Mediserve Information Systems, Inc.
- Decided: Dec 23, 2005 after 84 days
- Product code: MOD (Accessory To Continuous Ventilator (Respirator))
- Device class: 2
- Regulation: 21 CFR 868.5895
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K903702 (1990). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K963633: Ventnet; Central Monitoring Station, Puritan Bennett Corp. (1996) Summary page 1.

## Indications for use
The VentLink System is intended to be used in any clinical setting while interfaced to any specified or validated ventilator device. The VentLink system is intended to provide a secondary display of data received from an interfaced ventilator device to appropriately configured workstations and wireless laptop computers and to be made available to any interfaced hospital information system (HIS).

Source page: https://510kreport.com/device/K052751
Methodology: https://510kreport.com/methodology