K-number	K133722
Device name	ASTHMA MONITOR AM3
Applicant	Eresearch Technology
Product code	BZG
Device class	Class II
Decision date	May 8, 2014
Decision	Substantially Equivalent
Regulation	868.1840

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Source

View the full FDA submission: accessdata.fda.gov

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ASTHMA MONITOR AM3

Everything you need for a 510(k) submission. Nothing you don't.