K-number	K885149
Device name	NEEDLE INSERT FOR SOFT TISSUE BIOPSY DEVICE
Applicant	Hart Enterprises, Inc.
Product code	DWO
Device class	Class I
Decision date	Jan 26, 1989
Decision	Substantially Equivalent
Regulation	878.4800

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View the full FDA submission: accessdata.fda.gov

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NEEDLE INSERT FOR SOFT TISSUE BIOPSY DEVICE

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