K-number	K913141
Device name	MEGA MYELOGRAM KIT
Applicant	Megadyne Medical Products, Inc.
Product code	FMI
Device class	Class II
Decision date	Oct 17, 1991
Decision	Substantially Equivalent
Regulation	880.5570

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View the full FDA submission: accessdata.fda.gov

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MEGA MYELOGRAM KIT

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