Sooil Development Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sooil Development Co., Ltd. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Sooil Development Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in North Attleboro, US.
Historical record: 4 cleared submissions from 2000 to 2007. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Sooil Development Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sooil Development Co., Ltd.
4 devices
Cleared
Sep 04, 2007
DANA 3CC SYRINGE INSULIN RESERVOIR
General Hospital
105d
Cleared
Feb 02, 2007
DANA DIABECARE IIS
General Hospital
112d
Cleared
Aug 02, 2002
DANA DIABECARE II INSULIN PUMP & SUPERLINE-EASYRELEASE, SOFT-RELEASE-ST, &...
General Hospital
16d
Cleared
Aug 14, 2000
DANA DIABECARE
General Hospital
82d