K-number	K896041
Device name	GESCO DUAL LUMEN UMBILICATH II-DL
Applicant	Gesco Intl., Inc.
Product code	FOS
Device class	Class II
Decision date	Apr 17, 1990
Decision	Substantially Equivalent — Kit Device
Regulation	880.5200

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View the full FDA submission: accessdata.fda.gov

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GESCO DUAL LUMEN UMBILICATH II-DL

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