K-number	K080299
Device name	RESPIFIT S, MODEL RS-LR1001004
Applicant	Eumedics Medizintechnik Und Marketing GmbH
Product code	BWF
Device class	Class II
Decision date	Jan 13, 2009
Decision	Substantially Equivalent
Regulation	868.5690

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Source

View the full FDA submission: accessdata.fda.gov

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RESPIFIT S, MODEL RS-LR1001004

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