K-number	K990278
Device name	DAUM NEUROCUT NEUROBIOPSYNEEDLE
Applicant	Daum Corp.
Product code	KNW
Device class	Class II
Decision date	Mar 30, 1999
Decision	Substantially Equivalent
Regulation	876.1075

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View the full FDA submission: accessdata.fda.gov

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DAUM NEUROCUT NEUROBIOPSYNEEDLE

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