# K080926: Aeroeclipse Durable Breath Actuated Nebulizer

- Pathway: 510(k) (Traditional)
- Applicant: Trudell Medical Intl.
- Decided: Aug 12, 2008 after 132 days
- Product code: CAF (Nebulizer (Direct Patient Interface))
- Device class: 2
- Regulation: 21 CFR 868.5630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices 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.

## Most influential descendants
- K220145: Monaghan medical filtered mouthpiece kit (2023), 0 descendants of its own
- K173825: MC 300R* Nebulizer (2018), 0 descendants of its own

## Indications for use
The AeroEclipse® Durable Breath Actuated Nebulizer is a single patient, reusable device, intended to be used by patients who are under the care or treatment of a licensed health care provider or physician. The device is intended to be used by these patients to administer aerosolized medication prescribed by a physician or health care professional. The intended environments for use include the home, hospitals and clinics. The device may be used with a compressor capable of delivering a flow of 2.75 to 8 Ipm under an operating pressure of 15 to 50 psi.

Source page: https://510kreport.com/device/K080926
Methodology: https://510kreport.com/methodology