K-number	K791771
Device name	ORALUMINATOR III AUTO-LIGHT
Applicant	Midwest
Product code	EAY
Device class	Class I
Decision date	Nov 20, 1979
Decision	Substantially Equivalent
Regulation	872.4620

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View the full FDA submission: accessdata.fda.gov

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ORALUMINATOR III AUTO-LIGHT

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