K-number	K771658
Device name	IDENTOFLEX
Applicant	Cavitron Corp.
Product code	EHJ
Device class	Class I
Decision date	Sep 12, 1977
Decision	Substantially Equivalent
Regulation	872.6010

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View the full FDA submission: accessdata.fda.gov

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IDENTOFLEX

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