Convatec, A Division of E.R. Squibb & Sons, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Convatec, A Division of E.R. Squibb & Sons, LLC - FDA 510(k) Cleared ...
3
Total
3
Cleared
0
Denied
Convatec, A Division of E.R. Squibb & Sons, LLC has 3 FDA 510(k) cleared medical devices. Based in Skillman, US.
Historical record: 3 cleared submissions from 2007 to 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Convatec, A Division of E.R. Squibb & Sons, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Convatec, A Division of E.R. Squibb & Sons, LLC
3 devices
Cleared
Sep 04, 2009
SILVER IMPREGNATED HYDROFIBER DRESSING REINFORCED WITH NYLON (FLAT)
General & Plastic Surgery
214d
Cleared
May 02, 2008
AQUACEL HYDROFIBER WOUND DRESSING AND AG HYDROFIBER DRESSING
General & Plastic Surgery
80d
Cleared
Apr 16, 2007
AQUACEL HYDROFIBER DRESSING AND AQUACEL AG WITH HYDROFIBER SILVER IMPREGNATED...
General & Plastic Surgery
168d