K-number	K854197
Device name	IOSERT LENS IMPLANT INSTRUMENT
Applicant	Chiron Vision Corp.
Product code	KYB
Device class	Class I
Decision date	Jan 22, 1986
Decision	Substantially Equivalent
Regulation	886.4300

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View the full FDA submission: accessdata.fda.gov

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IOSERT LENS IMPLANT INSTRUMENT

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