K-number	K073185
Device name	APX21
Applicant	Techdent Technologies, Ltd.
Product code	LQY
Device class	Class U
Decision date	Mar 6, 2008
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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APX21

Everything you need for a 510(k) submission. Nothing you don't.