K-number	K993200
Device name	MD 420/440/460/470/480/490
Applicant	Isopure, Corp.
Product code	FIP
Device class	Class II
Decision date	Jan 24, 2000
Decision	Substantially Equivalent
Regulation	876.5665

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Source

View the full FDA submission: accessdata.fda.gov

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MD 420/440/460/470/480/490

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