K-number	K090670
Device name	MIDMARK M3 ULTRAFAST AUTOMATIC STERILIZER
Applicant	Midmark Corp.
Product code	FLE
Device class	Class II
Decision date	Jul 7, 2009
Decision	Substantially Equivalent
Regulation	880.6880

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View the full FDA submission: accessdata.fda.gov

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MIDMARK M3 ULTRAFAST AUTOMATIC STERILIZER

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