K-number	K062097
Device name	VERESS CANNULA AND MODULAR VERESS CANNULA
Applicant	PAJUNK GmbH Medizintechnologie
Product code	HET
Device class	Class II
Decision date	Oct 13, 2006
Decision	Substantially Equivalent
Regulation	884.1720

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View the full FDA submission: accessdata.fda.gov

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VERESS CANNULA AND MODULAR VERESS CANNULA

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