K-number	K072960
Device name	CDP 5000, MEDIA AND DISTRIBUTION CENTER, DIAGNET
Applicant	Cdp, Ltd.
Product code	LLZ
Device class	Class II
Decision date	Nov 8, 2007
Decision	Substantially Equivalent
Regulation	892.2050

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View the full FDA submission: accessdata.fda.gov

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CDP 5000, MEDIA AND DISTRIBUTION CENTER, DIAGNET

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