K-number	K895480
Device name	BLUNT NEEDLE PORT/I.V. PORT
Applicant	Applied Medical Technologies
Product code	FPA
Device class	Class II
Decision date	Dec 1, 1989
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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BLUNT NEEDLE PORT/I.V. PORT

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