K-number	K013812
Device name	SPIROLAB II, MODEL 29
Applicant	Sdi Diagnostics, Inc.
Product code	BZG
Device class	Class II
Decision date	Feb 11, 2002
Decision	Substantially Equivalent
Regulation	868.1840

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View the full FDA submission: accessdata.fda.gov

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SPIROLAB II, MODEL 29

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