K-number	K915390
Device name	3 LEAD EXTENSION WITH 2 INTERLINK INJECTION SITES
Applicant	Baxter Healthcare Corp
Product code	FPA
Device class	Class II
Decision date	Mar 12, 1992
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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3 LEAD EXTENSION WITH 2 INTERLINK INJECTION SITES

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