K-number	K901553
Device name	SURG-K SURGICAL KERATOMETER
Applicant	The Sanborn Co.
Product code	HLR
Device class	Class I
Decision date	Jul 20, 1990
Decision	Substantially Equivalent
Regulation	886.1350

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View the full FDA submission: accessdata.fda.gov

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SURG-K SURGICAL KERATOMETER

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