K-number	K023067
Device name	IMTEC SENDAX MDI ORTHO6 AND ORTHO8
Applicant	Imtec Corp.
Product code	DZE
Device class	Class II
Decision date	Dec 3, 2002
Decision	Substantially Equivalent
Regulation	872.3640

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View the full FDA submission: accessdata.fda.gov

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IMTEC SENDAX MDI ORTHO6 AND ORTHO8

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