Swiss American Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Swiss American Products, Inc. - FDA 510(k) Cleared Devices
4
Total
3
Cleared
0
Denied
Swiss American Products, Inc. has 3 FDA 510(k) cleared medical devices. Based in Dallas, US.
Historical record: 3 cleared submissions from 1994 to 2011. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Swiss American Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Swiss American Products, Inc.
4 devices
Cleared
Jun 16, 2011
ELTA WOUND CLEANSER
General & Plastic Surgery
177d
Cleared
Apr 23, 2008
ELTA ADVANCED WOUND WASH
General & Plastic Surgery
124d
Cleared
Aug 22, 2007
ELTA SILVER ANTIMICROBIAL WOUND GEL DRESSING, WOUND AND BURN, HYDROGEL W/DRUG...
General & Plastic Surgery
62d
Cleared
Jul 18, 1994
EUTRA GEL FOR WOUND DRESSING
General & Plastic Surgery
434d