# K190304: Kingon P2 Oxygen Concentrator

- Pathway: 510(k) (Traditional)
- Applicant: Qingdao Kingon Medical Science and Technology Co.
- Decided: Feb 29, 2020 after 382 days
- Product code: CAW (Generator, Oxygen, Portable)
- Device class: 2
- Regulation: 21 CFR 868.5440
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K111885 (2011). 1 ancestor in all.
2 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K111885: Simplygo Portable Oxygen Concentrator, Respironics, Inc. (2011) Summary page 4.

## Most influential descendants
- K242718: Portable Oxygen Concentrator (P2-TOC) (2025), 1 descendant of its own
- K252268: V series portable oxygen concentrator (V5, V5C, V6, V6C) (2025), 0 descendants of its own

## Indications for use
The Kingon P2 is for prescription use by patients requiring high concentrations of oxygen on a supplemental basis. It is small, portable, and is capable of continuous use in the home, institutional, and travel / mobile environments.

Source page: https://510kreport.com/device/K190304
Methodology: https://510kreport.com/methodology