Genzyme Biosurgery - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Genzyme Biosurgery has 4 FDA 510(k) cleared medical devices. Based in Fall River, US.
Historical record: 4 cleared submissions from 2002 to 2003. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Genzyme Biosurgery Filter by specialty or product code using the sidebar.
4 devices
Cleared
Jul 25, 2003
S-1150 PLEUR-EVAC SAHARA PLUS CONTINUOUS REINFUSION AUTOTRANSFUSION SYSTEM
Anesthesiology
67d
Cleared
Mar 27, 2003
MONODEK SYNTHETIC ABSORBABLE SURGICAL SUTURE
General & Plastic Surgery
65d
Cleared
Nov 25, 2002
RADLITE TISSUE RETRACTOR SYSTEM
General & Plastic Surgery
77d
Cleared
Aug 20, 2002
SAPH-LOOP LIGATING LOOP
General & Plastic Surgery
27d