K-number	K925626
Device name	MAXIMA PLUS HOLLOW FIBER OXYGENATOR
Applicant	Medtronic Vascular
Product code	DTZ
Device class	Class II
Decision date	Feb 5, 1993
Decision	Substantially Equivalent
Regulation	870.4350

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View the full FDA submission: accessdata.fda.gov

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MAXIMA PLUS HOLLOW FIBER OXYGENATOR

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