K-number	K892429
Device name	INJECTION PORT FOR---INTERMITTENT INJECTION
Applicant	The Medi-Dose Group
Product code	FPA
Device class	Class II
Decision date	Jul 25, 1989
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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INJECTION PORT FOR---INTERMITTENT INJECTION

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