# K952429: Res Care Auto Set Clinical, Portable System, Portable 2 System

- Pathway: 510(k) (Traditional)
- Applicant: Rescare, Ltd.
- Decided: Jul 2, 1996 after 405 days
- Product code: BZD (Ventilator, Non-Continuous (Respirator))
- Device class: 2
- Regulation: 21 CFR 868.5905
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
19 later devices descend from it; 1 cites it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K092186: Vpap TX (2009), 18 descendants of its own
- K102513: S9 Vpap ST with H5I (2011), 11 descendants of its own
- K113288: Vpap ST-a (2012), 7 descendants of its own
- K102586: S9 Vpap Adapt with H5I (2011), 6 descendants of its own
- K113801: Vpap Adapt (2012), 5 descendants of its own

Source page: https://510kreport.com/device/K952429
Methodology: https://510kreport.com/methodology