K-number	K980003
Device name	M500-100 SHARPS CONTAINER
Applicant	Imagination Medical, Inc.
Product code	FMI
Device class	Class II
Decision date	Mar 13, 1998
Decision	Substantially Equivalent
Regulation	880.5570

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View the full FDA submission: accessdata.fda.gov

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M500-100 SHARPS CONTAINER

Everything you need for a 510(k) submission. Nothing you don't.