Baldur Systems Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Baldur Systems Corp. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Baldur Systems Corp. has 6 FDA 510(k) cleared medical devices. Based in Hayward, US.
Historical record: 6 cleared submissions from 1989 to 1998. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Baldur Systems Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Baldur Systems Corp.
6 devices
Cleared
Aug 11, 1998
OPERATING ROOM TOWELS
General Hospital
81d
Cleared
Feb 10, 1998
BALDUR NON-STERILE COTTON SPONGES
General & Plastic Surgery
83d
Cleared
Sep 11, 1989
PATIENT EXAMINATION GLOVES (LATEX)
General Hospital
153d
Cleared
May 25, 1989
LATEX EXAM GLOVES (MFG. KOON SENG SDN BHD)
General Hospital
63d
Cleared
May 12, 1989
VINYL EXAM GLOVES (MFG. SUN FLOWER GLOVE CO.)
General Hospital
50d
Cleared
May 12, 1989
LATEX EXAM GLOVES (MFG. RINDUMAS SDN BHD)
General Hospital
50d