H.W. Andersen Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
H.W. Andersen Products, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
H.W. Andersen Products, Inc. has 5 FDA 510(k) cleared medical devices. Based in Oyster Bay, US.
Historical record: 5 cleared submissions from 1987 to 1994. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by H.W. Andersen Products, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - H.W. Andersen Products, Inc.
5 devices
Cleared
Dec 30, 1994
AN-10S ANDERSEN TUBE WITH STYLET
Gastroenterology & Urology
396d
Cleared
Sep 21, 1987
AN3200 DOUBILET DRAIN
Gastroenterology & Urology
90d
Cleared
Jul 23, 1987
AN3000 MAHONEY DRAIN
General & Plastic Surgery
30d
Cleared
Jul 21, 1987
AN3500 WORTH DRAIN
General & Plastic Surgery
28d
Cleared
Jul 21, 1987
AN3100 MULHOLLAND DRAIN
General & Plastic Surgery
28d