K-number	K122519
Device name	DIO UF HSA INTERNAL SUB-MERGED IMPLANT SYSTEM
Applicant	Dio Corporation
Product code	DZE
Device class	Class II
Decision date	May 21, 2013
Decision	Substantially Equivalent
Regulation	872.3640

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Source

View the full FDA submission: accessdata.fda.gov

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DIO UF HSA INTERNAL SUB-MERGED IMPLANT SYSTEM

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