K-number	K955558
Device name	GIP/MEDI-GLOBE SCLEROTHERAPY NEEDLES
Applicant	Medi-Globe Corp.
Product code	FBK
Device class	Class II
Decision date	Feb 29, 1996
Decision	Substantially Equivalent
Regulation	876.1500

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GIP/MEDI-GLOBE SCLEROTHERAPY NEEDLES

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