# K872037: Aerochamber

- Pathway: 510(k) (Traditional)
- Applicant: Monaghan Medical Corp.
- Decided: Jul 24, 1987 after 58 days
- Product code: BYP (Mouthpiece, Breathing)
- Device class: 1
- Regulation: 21 CFR 868.5620
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 4 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K960593: Smartmist Asthma Managment System, Smartmist, Model Number SM-100/Smartmist Spirometry Airway, Model Number SA-100 (1996), 1 descendant of its own
- K130598: Inspirachamber Anti-Static Valved Holding Chamber (2013), 0 descendants of its own
- K051284: MD Turbo (2005), 0 descendants of its own
- K020944: Vortex Valved Holding Chamber (2002), 0 descendants of its own
- K964130: Aerogear Asthma Action Kit (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K872037
Methodology: https://510kreport.com/methodology