# K254104: ResScan Essentials

- Pathway: 510(k) (Traditional)
- Applicant: Resmed Corp
- Decided: May 27, 2026 after 159 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
Longest line of descent: 8 generations back to K971260 (1997). 14 ancestors in all.
No later device cites it as a predicate yet.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K140054: Rescan, Resmed, Ltd. (2014) Summary page 6.

## Indications for use
ResScan Essentials is intended to augment the standard follow-up care of patients by transferring and analyzing machine and therapeutic information from ResMed compatible therapy devices to the ResScan Essentials application. ResScan Essentials is intended to be used by clinicians.

Source page: https://510kreport.com/device/K254104
Methodology: https://510kreport.com/methodology