K-number	K790912
Device name	ARIDYNE 3500
Applicant	Timeter Instrument Corp.
Product code	BTI
Device class	Class II
Decision date	May 21, 1979
Decision	Substantially Equivalent
Regulation	868.6250

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View the full FDA submission: accessdata.fda.gov

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ARIDYNE 3500

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