K-number	K031643
Device name	SPIROTEL, MODEL 29-1020
Applicant	Sdi Diagnostics, Inc.
Product code	BZG
Device class	Class II
Decision date	Dec 9, 2003
Decision	Substantially Equivalent
Regulation	868.1840

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View the full FDA submission: accessdata.fda.gov

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SPIROTEL, MODEL 29-1020

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