K-number	K091248
Device name	MAXEMS, MODELS 1000 AND 2000
Applicant	Bio Protech, Inc.
Product code	IPF
Device class	Class II
Decision date	Nov 30, 2009
Decision	Substantially Equivalent
Regulation	890.5850

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View the full FDA submission: accessdata.fda.gov

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MAXEMS, MODELS 1000 AND 2000

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