K-number	K091320
Device name	SPECTRA SP II, SPECTRA DENTA II
Applicant	Lutronic Corporation
Product code	GEX
Device class	Class II
Decision date	Aug 19, 2009
Decision	Substantially Equivalent
Regulation	878.4810

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View the full FDA submission: accessdata.fda.gov

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SPECTRA SP II, SPECTRA DENTA II

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