# K903010: Continuous Volume Ventilator Model LP10

- Pathway: 510(k) (Traditional)
- Applicant: Aequitron Medical, Inc.
- Decided: Nov 30, 1990 after 142 days
- Product code: CBK (Ventilator, Continuous, Facility Use)
- Device class: 2
- Regulation: 21 CFR 868.5895
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
4 later devices descend from it; 1 cites it directly.
0 of 5 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
- K990177: Nellcor Puritan Bennett Achieva Ventilator and Report Generator (1999), 3 descendants of its own
- K034032: PLV Continuum Ventilator, Model P2000 (2004), 1 descendant of its own
- K081845: IVENT101 (2009), 0 descendants of its own
- K040712: Air Safety Hepa, Model 3500 (2004), 0 descendants of its own

Source page: https://510kreport.com/device/K903010
Methodology: https://510kreport.com/methodology