# K063813: Ventlab Nasal CO2 Sampling/O2 Delivery Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Ventlab Corp.
- Decided: Mar 26, 2008 after 460 days
- Product code: CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase)
- Device class: 2
- Regulation: 21 CFR 868.1400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
The Ventlab End-Tidal C02 Nasal Cannula is an accessory to a carbon dioxide analyzer used when there is a need to measure the percentage of exhaled carbon dioxide of a non-intubated patient while administering oxygen during inhalation.

Source page: https://510kreport.com/device/K063813
Methodology: https://510kreport.com/methodology