K-number	K923127
Device name	NEEDLE-PRO CARTRIDGE
Applicant	Concord/Portex
Product code	FMI
Device class	Class II
Decision date	Apr 29, 1993
Decision	Substantially Equivalent
Regulation	880.5570

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Source

View the full FDA submission: accessdata.fda.gov

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NEEDLE-PRO CARTRIDGE

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