K-number	K040913
Device name	NGDI (NEXT GENERATION DIAGNOSTIC INSTRUMENT)
Applicant	Bausch & Lomb
Product code	MXK
Device class	Class II
Decision date	Jul 23, 2004
Decision	Substantially Equivalent
Regulation	886.1850

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Source

View the full FDA submission: accessdata.fda.gov

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NGDI (NEXT GENERATION DIAGNOSTIC INSTRUMENT)

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