K-number	K082016
Device name	GDX VCC WITH ECC SOFTWARE
Applicant	Carl Zeiss Meditec, Inc.
Product code	MYC
Device class	Class II
Decision date	Aug 10, 2009
Decision	Substantially Equivalent
Regulation	886.1570

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Source

View the full FDA submission: accessdata.fda.gov

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GDX VCC WITH ECC SOFTWARE

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