# K160630: Invacare Platinum Mobile Oxygen Concentrator

- Pathway: 510(k) (Traditional)
- Applicant: Invacare Corporation
- Decided: Sep 27, 2016 after 204 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: 3 generations back to K020324 (2002). 3 ancestors in all.
1 later device descends 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)
- K071928: The Invacare Flyer, Model Ipc 100, Invacare Corp. (2007) Summary page 4.

## Most influential descendants
- K191159: Concentrator with Single battery pack, carry bag with shoulder strap, back pack shoulder straps, A, POC1 USB Bluetooth Dongle, POC1 Invacare Mobile Medical Application Accessory for use on iOS and Android Devices, Invacare Platinum Mobile Oxygen Concentrator with Connectivity (2019), 0 descendants of its own

## Indications for use
The Invacare® Platinum™ Mobile Oxygen Concentrator is intended to provide supplemental oxygen to patients with respiratory disorders. The device can be used in a home, institution, vehicle, or other environments outside the home.

Source page: https://510kreport.com/device/K160630
Methodology: https://510kreport.com/methodology