Tridak Division of Indicon, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Tridak Division of Indicon, Inc. Gastroenterology & Urology ✕
5 devices
Cleared
Jun 07, 1990
NONIMPLANTED ELECTRICAL CONTINENCE DEVICE
Gastroenterology & Urology
465d
Cleared
Jan 10, 1986
LABORIE FIBEROPTIC PRESSURE SENSOR & INTERFACE
Gastroenterology & Urology
175d
Cleared
Oct 17, 1985
LABORIE URODYNAMICS PROCESSOR
Gastroenterology & Urology
104d
Cleared
Aug 09, 1984
R.L. MEDICAL TWIN LIGHT SOURCE
Gastroenterology & Urology
35d
Cleared
Apr 13, 1984
LABORIE FIBREOPTIC LIGHT CABLE
Gastroenterology & Urology
63d