# K040726: Ventlab Nasal Cpap Cannula

- Pathway: 510(k) (Traditional)
- Applicant: Ventlab Corp.
- Decided: Jun 3, 2004 after 73 days
- Product code: BZD (Ventilator, Non-Continuous (Respirator))
- Device class: 2
- Regulation: 21 CFR 868.5905
- 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 Nasal CPAP Cannula is an accessory to positive pressure ventilation devices for patients suffering from Obstructive Sleep Apnea requiring positive pressure breathing therapy (i.e., CPAP, BiLevel). Federal (USA) law restricts this device to sale by or on the order of a physician.

Source page: https://510kreport.com/device/K040726
Methodology: https://510kreport.com/methodology