# K071928: The Invacare Flyer, Model Ipc 100

- Pathway: 510(k) (Traditional)
- Applicant: Invacare Corp.
- Decided: Dec 12, 2007 after 153 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: 2 generations back to K020324 (2002). 2 ancestors in all.
3 later devices descend from it; 2 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K032818: Inogen One Oxygen Concentrator, Inogen, Inc. (2004) Summary page 1.

## Most influential descendants
- K160630: Invacare Platinum Mobile Oxygen Concentrator (2016), 1 descendant of its own
- 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
- K103563: Precision Portable Oxygen Concentration Model 4150 (2011), 0 descendants of its own

## Indications for use
The Invacare Flyer (Model XPOI00) is intended to be used by patients with respiratory disorders who require supplemental oxygen. It supplies a high concentration of supplemental oxygen and is used with a nasal cannula to channel oxygen from the concentrator to the patient. The Invacare Flyer can be used in a home, institution, vehicle and various mobile environments. The Invacare Flyer does not nor is it intended to sustain or support life.

Source page: https://510kreport.com/device/K071928
Methodology: https://510kreport.com/methodology