K-number	K990803
Device name	MEDISYSTEMS BUTTONHOLE NEEDLE SETS
Applicant	Medisystems Corp.
Product code	FIE
Device class	Class II
Decision date	Jan 6, 2000
Decision	Substantially Equivalent
Regulation	876.5540

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Source

View the full FDA submission: accessdata.fda.gov

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MEDISYSTEMS BUTTONHOLE NEEDLE SETS

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