K-number	K896622
Device name	VISITEC VITRECTOMY UNIT
Applicant	Visitec Co.
Product code	HKP
Device class	Class II
Decision date	Apr 4, 1990
Decision	Substantially Equivalent
Regulation	886.4150

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View the full FDA submission: accessdata.fda.gov

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VISITEC VITRECTOMY UNIT

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