K-number	K120170
Device name	PROCARE PLUS VITRECTOMY SYSTEM
Applicant	Visioncare Devices, Inc.
Product code	HQE
Device class	Class II
Decision date	May 30, 2012
Decision	Substantially Equivalent
Regulation	886.4150

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Source

View the full FDA submission: accessdata.fda.gov

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PROCARE PLUS VITRECTOMY SYSTEM

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