FDA 510(k) Applications Submitted by DAUM CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K990278	01/28/1999	DAUM NEUROCUT NEUROBIOPSYNEEDLE	DAUM CORP.
K974574	12/08/1997	DAUM NEUROPUNCTURE NEEDLE	DAUM CORP.
K974575	12/08/1997	DAUM ASPIRATIONBIOPSY NEEDLE	DAUM CORP.
K974576	12/08/1997	DAUM BIOPSYGUN	DAUM CORP.
K974631	12/12/1997	DAUM NEUROBIOPSY NEEDLE	DAUM CORP.
K981320	04/10/1998	DAUM BONE BIOPSY SET	DAUM CORP.