K-number	K112188
Device name	PIEZOTOME SOLO
Applicant	Satelec - Acteon, Inc.
Product code	DZI
Device class	Class II
Decision date	Feb 3, 2012
Decision	Substantially Equivalent
Regulation	872.4120

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Source

View the full FDA submission: accessdata.fda.gov

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PIEZOTOME SOLO

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