K-number	K924779
Device name	BURTON KERATOMETER - MODLE 2040
Applicant	R.H. Burton Co.
Product code	HJB
Device class	Class I
Decision date	Apr 5, 1993
Decision	Substantially Equivalent
Regulation	886.1450

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View the full FDA submission: accessdata.fda.gov

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BURTON KERATOMETER - MODLE 2040

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