K-number	K120577
Device name	MEDIKRO SPIROSTAR, M929 Medikro Spirostar USB and M921 Medikro SpiroStar DX
Applicant	Medikro OY
Product code	BZG
Device class	Class II
Decision date	Jun 24, 2015
Decision	Substantially Equivalent
Regulation	868.1840

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View the full FDA submission: accessdata.fda.gov

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MEDIKRO SPIROSTAR, M929 Medikro Spirostar USB and M921 Medikro SpiroStar DX

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