ClearanceBrief
Company ยท US

Daum Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1997 to 2001. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KNWInstrument, Biopsy9
LNHSystem, Nuclear Magnetic Resonance Imaging1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 22, 2001K010037DAUM DOUBLE-SHOOT BISOPSY GUN
Daum GmbH
KNW
Jun 25, 1999K991366DAUM MRI/CONVENTIONAL BIOPSY KIT
Daum GmbH
KNW
Apr 28, 1999K990782DAUM NEUROGATE TROCAR
Daum GmbH
KNW
Mar 30, 1999K990278DAUM NEUROCUT NEUROBIOPSYNEEDLE
Daum Corp.
KNW
Jun 29, 1998K981320DAUM BONE BIOPSY SET
Daum Corp.
KNW
Mar 9, 1998K974631DAUM NEUROBIOPSY NEEDLE
Daum Corp.
KNW
Mar 6, 1998K974576DAUM BIOPSYGUN
Daum Corp.
KNW
Mar 6, 1998K974575DAUM ASPIRATIONBIOPSY NEEDLE
Daum Corp.
KNW
Mar 6, 1998K974574DAUM NEUROPUNCTURE NEEDLE
Daum Corp.
KNW
Mar 12, 1997K970037TARGOGRID
Daum GmbH, DE
LNH

Latest recalls

DateFirm and productCodeLinked 510(k)
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