K-number	K092085
Device name	ISPIRA RESUSCITATION UNIT
Applicant	Neoforce Group, Inc.
Product code	BTL
Device class	Class II
Decision date	Oct 7, 2009
Decision	Substantially Equivalent
Regulation	868.5925

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Source

View the full FDA submission: accessdata.fda.gov

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ISPIRA RESUSCITATION UNIT

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