Biosurgical Corp. - FDA 510(k) Cleared Devices
Recent clearances: SEALOUETTE FIBRIN SEALANT APPLICATOR, BIOSURGICAL, CORP. MULTI CHAMBER SUCTION SYRINGE
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Biosurgical Corp. General Hospital ✕
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