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I N T R O D U C T I O N
This patient manual will familiarize you with the LifeChoice Portable Oxygen Concentrator
(POC) and its accessories. Be sure to thoroughly read all of the information in this manual in
its entirety before using the LifeChoice POC. The LifeChoice POC is an internally powered,
type BF device when powered by the internal battery and a Class II, Type BF device when
connected to the external C power supply, DC power supply or rechargeable battery. The
essential performance of the LifeChoice POC is to provide oxygen at a volume that remains
within tolerance (the tolerance was defined based on technical judgement from within the
manufacturer' s expertise in this specific medical application). In addition, the device' s ability
to detect certain error conditions (such as low concentration or no breath) and create an
alarm is also considered a part of essential performance.
P P L I C
T I O N
This manual applies to the LifeChoice POC
INDIC TIONS FOR USE: The LifeChoice Oxygen Concentrator is used on a prescriptive basis by
patients who are diagnosed as requiring supplemental oxygen. This oxygen concentrator will provide
supplemental, high concentration oxygen to these patients. It is not life supporting nor life sustaining. It
may be used continuously in a home, institution or travel environment. The LifeChoice is also portable.
The LifeChoice POC is F
sticker is located on the bottom of the LifeChoice POC. F
is listed as Inova Labs LifeChoice. Every airline has specific information
required for traveling with oxygen. Before traveling, review your airline's
specific requirements.
S Y M B O L D E S C R I P T I O N S
Symbol
Description
Manufacturer
Humidity
Limitation
Waste Disposal
Catalogue Number
REF
Keep Dry
REF
XYC100.
approved for air travel. The required F
Symbol
Description
Temperature
Limitation
Gas Flow
GAS FLOW
DC Power
Class II Equipment
General Warning,
!
Caution,
Risk of Danger
Danger, No Smoking
or Open Flame
Symbol
Description
Radio
Frequency
Type BF
pplied Part
Device that has
conductive contact
with patient
CE Marking
of Conformity
EU uthorized
Representative
approval
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