K-number	K936029
Device name	NON-CORNING (HUBER) NEEDLE
Applicant	Therex Corp.
Product code	FMI
Device class	Class II
Decision date	Feb 4, 1994
Decision	Substantially Equivalent
Regulation	880.5570

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View the full FDA submission: accessdata.fda.gov

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NON-CORNING (HUBER) NEEDLE

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