K-number	K113333
Device name	KIMBERLY-CLARK KIM VENT MICROCUFF ENDOTRACHEAL TUBE FOR ADULTS
Applicant	Kimberly-Clark Corporation
Product code	BTR
Device class	Class II
Decision date	May 11, 2012
Decision	Substantially Equivalent
Regulation	868.5730

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View the full FDA submission: accessdata.fda.gov

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KIMBERLY-CLARK KIM VENT MICROCUFF ENDOTRACHEAL TUBE FOR ADULTS

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