Daum Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Daum Corp. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Daum Corp. has 6 FDA 510(k) cleared medical devices. Based in Crofton, US.
Historical record: 6 cleared submissions from 1998 to 1999. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Daum Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Daum Corp.
6 devices
Cleared
Mar 30, 1999
DAUM NEUROCUT NEUROBIOPSYNEEDLE
Gastroenterology & Urology
61d
Cleared
Jun 29, 1998
DAUM BONE BIOPSY SET
Gastroenterology & Urology
80d
Cleared
Mar 09, 1998
DAUM NEUROBIOPSY NEEDLE
Gastroenterology & Urology
87d
Cleared
Mar 06, 1998
DAUM NEUROPUNCTURE NEEDLE
Gastroenterology & Urology
88d
Cleared
Mar 06, 1998
DAUM ASPIRATIONBIOPSY NEEDLE
Gastroenterology & Urology
88d
Cleared
Mar 06, 1998
DAUM BIOPSYGUN
Gastroenterology & Urology
88d