K-number	K915265
Device name	CDI(TM) H/S CUVETTE, MODIFICATION
Applicant	3M Company
Product code	DRY
Device class	Class II
Decision date	Jan 15, 1992
Decision	Substantially Equivalent
Regulation	870.4330

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View the full FDA submission: accessdata.fda.gov

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CDI(TM) H/S CUVETTE, MODIFICATION

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