K-number	K904909
Device name	I/A VITROPHAGE MODEL YPR 2001
Applicant	Visioncare Devices, Inc.
Product code	HQE
Device class	Class II
Decision date	Jan 28, 1991
Decision	Substantially Equivalent
Regulation	886.4150

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View the full FDA submission: accessdata.fda.gov

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I/A VITROPHAGE MODEL YPR 2001

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