K-number	K944616
Device name	KERATRON CORNEAL TOPOGRAPHER
Applicant	Alliance Medical Marketinig
Product code	HLQ
Device class	Class I
Decision date	Nov 22, 1994
Decision	Substantially Equivalent
Regulation	886.1350

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View the full FDA submission: accessdata.fda.gov

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KERATRON CORNEAL TOPOGRAPHER

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