# K082983: Resscan-Pro

- Pathway: 510(k) (Traditional)
- Applicant: Resmed, Ltd.
- Decided: Jan 2, 2009 after 88 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: 6 generations back to K971260 (1997). 12 ancestors in all.
13 later devices descend from it; 1 cites it directly.
0 of 26 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050775: Resscan, Resmed, Ltd. (2005) Summary page 1.

## Most influential descendants
- K093684: Easycare Online (2010), 12 descendants of its own
- K123557: Easycare Online (2013), 9 descendants of its own
- K132371: Easycare Online (2013), 8 descendants of its own
- K152356: Sapphire (2016), 4 descendants of its own
- K181053: Care Orchestrator (2019), 1 descendant of its own

## Indications for use
ResScan-Pro is intended to augment the standard follow-up care of patients by providing transfer of machine and therapeutic information, including the ability to remotely change settings. It is intended to be used by Clinicians in conjunction with ResMed compatible flow generators.

Source page: https://510kreport.com/device/K082983
Methodology: https://510kreport.com/methodology