K-number	K862610
Device name	ULTRA-VUE SPINAL TYPE BIOPSY NEEDLE
Applicant	Bd Becton Dickinson Vacutainer Systems Preanalytic
Product code	FMI
Device class	Class II
Decision date	Feb 4, 1987
Decision	Substantially Equivalent
Regulation	880.5570

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View the full FDA submission: accessdata.fda.gov

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ULTRA-VUE SPINAL TYPE BIOPSY NEEDLE

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