Welcon, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Welcon, Inc. - FDA 510(k) Cleared Devices
8
Total
7
Cleared
0
Denied
Welcon, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1981 to 2001.
Browse the FDA 510(k) cleared devices submitted by Welcon, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Welcon, Inc.
8 devices
Cleared
May 01, 2001
WELCON STERILE WATER FOR DEVICE IRRIGATION
General Hospital
181d
Cleared
Feb 05, 1998
STERILE WATER FOR DEVICE IRRIGATION/ STERILE SALINE FOR DEVICE IRRIGATION
General Hospital
128d
Cleared
Jul 29, 1997
WELCON HUE-VU URINARY DRAINAGE BAG
Gastroenterology & Urology
77d
Cleared
Dec 04, 1991
WOMEN AND INFANT'S DELIVERY PACK
Obstetrics & Gynecology
159d
Cleared
Nov 29, 1990
ACCORDE(R) IRRIGATING SYRINGE/PROCEDURE TRAY
Gastroenterology & Urology
83d
Cleared
Aug 10, 1989
WELCON LIGHT HANDLE
General & Plastic Surgery
21d
Cleared
Mar 17, 1983
STERILE CATHERIZATION PROCEDURE TRAYS
Gastroenterology & Urology
42d
Cleared
Nov 20, 1981
STERILE IRRIGATING SYRINGES, KITS,TRAY
General Hospital
23d