K-number	K953827
Device name	GIP/MEDI-GLOBE ERCP CATHETERS
Applicant	Medi-Globe Corp.
Product code	FGE
Device class	Class II
Decision date	Sep 1, 1995
Decision	Substantially Equivalent
Regulation	876.5010

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View the full FDA submission: accessdata.fda.gov

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GIP/MEDI-GLOBE ERCP CATHETERS

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