K-number	K981432
Device name	GOLDMAN MANUAL TONOMETER
Applicant	Golden Vision, Inc.
Product code	HKY
Device class	Class II
Decision date	Jan 12, 1999
Decision	Substantially Equivalent
Regulation	886.1930

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View the full FDA submission: accessdata.fda.gov

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GOLDMAN MANUAL TONOMETER

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