Biosurgical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biosurgical Corp. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Biosurgical Corp. has 4 FDA 510(k) cleared medical devices. Based in Pleasanton, US.
Historical record: 4 cleared submissions from 1997 to 2000. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Biosurgical Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biosurgical Corp.
4 devices
Cleared
May 03, 2000
MULTI LUMEN SUCTION SYRINGE SPRAY DISPENSER
General Hospital
83d
Cleared
Jan 31, 2000
SEALOUETTE FIBRIN SEALANT EXTENDED DROPLET APPLICATOR, MODEL TE-1
General Hospital
24d
Cleared
Oct 08, 1999
SEALOUETTE FIBRIN SEALANT APPLICATOR
General Hospital
86d
Cleared
Sep 08, 1997
BIOSURGICAL, CORP. MULTI CHAMBER SUCTION SYRINGE
General Hospital
294d