# K102404: Provent Professional Sleep Apnea Therapy (Provent 80); Provent Professional Sleep Apnea Therapy (Provent 50)

- Pathway: 510(k) (Traditional)
- Applicant: Ventus Medical, Inc.
- Decided: Dec 2, 2010 after 100 days
- Product code: OHP (Expiratory Resistance Valve, Intranasal, For Obstructive Sleep Apnea)
- Device class: 2
- Regulation: 21 CFR 872.5570
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K953930 (1996). 78 ancestors in all.
2 later devices descend from it; 2 cite it directly.
0 of 81 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071560: Provent Nasal Dilator, Model BR2, Ventus Medical, Inc. (2008) Summary page 1.
- K090398: Provent Professional Sleep Apnea Therapy, Ventus Medical, Inc. (2009) Summary page 1.

## Most influential descendants
- K180619: Bongo (2018), 1 descendant of its own
- K191728: ULTepap Expiratory Positive Airway Pressure (EPAP) Device (2020), 0 descendants of its own

## Indications for use
The PROVENT® Sleep Apnea Therapy Device is indicated for use in the treatment of obstructive sleep apnea (OSA).

Source page: https://510kreport.com/device/K102404
Methodology: https://510kreport.com/methodology