Sween Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sween Corp. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Sween Corp. has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 4 cleared submissions from 1981 to 1993. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Sween Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sween Corp.
4 devices
Cleared
Jul 08, 1993
SWEEN WOUND CARE-COLLAGEN WOUND DRESSING
General & Plastic Surgery
198d
Cleared
Mar 02, 1992
CRITIC-AID WOUND DRESSING
General & Plastic Surgery
270d
Cleared
May 07, 1984
SWEEN-A-PEEL PERISTOMAL WAFERS
Gastroenterology & Urology
76d
Cleared
Apr 17, 1981
SWEEN UNIVERSAL BED RAIL PADS
General Hospital
21d