# K070674: Aerochamber Plus Anti-Static Valved Holding Chamber with Flow-VU Inspiratory Flow Indicator

- Pathway: 510(k) (Special)
- Applicant: Trudell Medical Intl.
- Decided: Apr 11, 2007 after 30 days
- Product code: NVP (Holding Chambers, 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.
6 later devices descend from it; 5 cite it directly.
0 of 7 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
- K091862: Nessi Spacer (2009), 1 descendant of its own
- K122252: Space Chamber Plus Compact Space Chamber Plus (2013), 0 descendants of its own
- K101348: Agachamber Spacer (2011), 0 descendants of its own
- K101136: Fisio Chamber Space (2011), 0 descendants of its own
- K101532: Nessi Otc Spacer (2010), 0 descendants of its own

## Indications for use
The AeroChamber Plus®aVHC with Flow-Vu® IFI is 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 from most pressurized Metered Dose Inhalers, prescribed by a physician or health care professional. The intended environments for use include the home, hospitals and clinics.

Source page: https://510kreport.com/device/K070674
Methodology: https://510kreport.com/methodology