K-number	K001708
Device name	PROFOX SOFTWARE, MODEL 920M-41
Applicant	Respironics Georgia, Inc.
Product code	DQA
Device class	Class II
Decision date	Mar 1, 2001
Decision	Substantially Equivalent
Regulation	870.2700

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View the full FDA submission: accessdata.fda.gov

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PROFOX SOFTWARE, MODEL 920M-41

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