K-number	K963972
Device name	NEO-CARE DUAL LUMEN UMBILICAL CATHETER
Applicant	Klein-Baker Medical, Inc.
Product code	FOS
Device class	Class II
Decision date	Dec 24, 1996
Decision	Substantially Equivalent
Regulation	880.5200

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View the full FDA submission: accessdata.fda.gov

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NEO-CARE DUAL LUMEN UMBILICAL CATHETER

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