K-number	K872506
Device name	MELANITE I
Applicant	Aura Lens Products
Product code	HQG
Device class	Class I
Decision date	Jul 27, 1987
Decision	Substantially Equivalent
Regulation	886.5844

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View the full FDA submission: accessdata.fda.gov

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MELANITE I

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