K-number	K032971
Device name	TIDAL WAVE SP MODEL 710/715 AND 715
Applicant	Respironics Novametrix, Inc.
Product code	DQA
Device class	Class II
Decision date	Aug 26, 2004
Decision	Substantially Equivalent
Regulation	870.2700

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View the full FDA submission: accessdata.fda.gov

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TIDAL WAVE SP MODEL 710/715 AND 715

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