K-number	K092530
Device name	SPRYTIE, MODELS ST001, ST002 AND ST003
Applicant	Russell B. Walther
Product code	DZK
Device class	Class II
Decision date	Apr 2, 2010
Decision	Substantially Equivalent
Regulation	872.4880

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View the full FDA submission: accessdata.fda.gov

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SPRYTIE, MODELS ST001, ST002 AND ST003

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