Andersen Products, Inc. is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Andersen Products, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ANDERSEN NASOGASTRIC TUBE WITH STYLET, MODELS AN 11S, 13S, 14S & 18S, ANDERSEN INTESTINAL TUBE, MILLER-ABBOTT TYPE (AN 22)
2
Total
2
Cleared
0
Denied
Andersen Products, Inc. has 2 FDA 510(k) cleared medical devices. Based in Haw River, US.
Historical record: 2 cleared submissions from 2001 to 2002. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Andersen Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Andersen Products, Inc.
2 devices