K-number	K992610
Device name	GENDEX 765DC, MODEL 110-0154
Applicant	Dentsply Intl.
Product code	EHD
Device class	Class II
Decision date	Sep 7, 1999
Decision	Substantially Equivalent
Regulation	872.1800

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View the full FDA submission: accessdata.fda.gov

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GENDEX 765DC, MODEL 110-0154

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