K-number	K841299
Device name	BIERMAN BIOPSY NEEDLE
Applicant	Popper & Sons, Inc.
Product code	GDM
Device class	Class I
Decision date	May 2, 1984
Decision	Substantially Equivalent
Regulation	878.4800

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View the full FDA submission: accessdata.fda.gov

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BIERMAN BIOPSY NEEDLE

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