Sscor is one of 20377 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sscor - FDA 510(k) Cleared Devices
Recent clearances: S-SCORT...JR QUICKDRAW, MODEL 2400, S-SCORT (2500), S-SCORT
5
Total
5
Cleared
0
Denied
Sscor has 5 FDA 510(k) cleared medical devices. Based in Sun Valley, US.
Historical record: 5 cleared submissions from 1994 to 2004. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Sscor Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Sscor
5 devices
Cleared
May 18, 2004
S-SCORT...JR QUICKDRAW, MODEL 2400
General & Plastic Surgery
15d
Cleared
Mar 05, 1997
S-SCORT (2500)
General & Plastic Surgery
79d
Cleared
Jun 16, 1995
S-SCORT
General & Plastic Surgery
8d
Cleared
Apr 25, 1995
SSCOR/BOARD ..3 MODEL 23000 PRE-ASSEMBLED SUCTION SYSTEM FOR PATIENT...
General Hospital
81d
Cleared
Dec 22, 1994
S-SCORT(R)DUET MODEL 2014 PORTABLE SUCTION PUMP
General & Plastic Surgery
17d