K-number	K070569
Device name	SM INTERNAL./EXTERNAL IMPLANT SYSTEM
Applicant	Dio Department Dsi, Inc.
Product code	DZE
Device class	Class II
Decision date	Nov 8, 2007
Decision	Substantially Equivalent
Regulation	872.3640

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View the full FDA submission: accessdata.fda.gov

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SM INTERNAL./EXTERNAL IMPLANT SYSTEM

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