Surgimed Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Surgimed Corp. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1981 to 1985. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Surgimed Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Surgimed Corp.
5 devices
Cleared
Apr 25, 1985
SURGIMED - SURGICAL BLADES
General & Plastic Surgery
34d
Cleared
Jul 13, 1984
SILVERTORQUE CEREBRAL CATHETER
Cardiovascular
141d
Cleared
Jun 13, 1984
SILVERTORQUE CARDIAC CATHETERS
Cardiovascular
111d
Cleared
Jun 11, 1984
SILVERTORQUE VISCERAL CATHETER
Cardiovascular
109d
Cleared
Jul 28, 1981
BALLOON CATHETER
General & Plastic Surgery
137d