Tridak Division of Indicon, Inc.
Tridak Division of Indicon, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 1990.
Top product codes for Tridak Division of Indicon, Inc.
Recent clearances by Tridak Division of Indicon, Inc.
- K891007 — NONIMPLANTED ELECTRICAL CONTINENCE DEVICE
- K860744 — OPTHALMIC SURGICAL INSTRUMENTS
- K853059 — LABORIE FIBEROPTIC PRESSURE SENSOR & INTERFACE
- K852856 — LABORIE URODYNAMICS PROCESSOR
- K851934 — CYTOLOGICAL CERVICAL SPATULA THE MULTI-SPATULA
- K842609 — R.L. MEDICAL TWIN LIGHT SOURCE
- K840605 — LABORIE FIBREOPTIC LIGHT CABLE
Data sourced from openFDA. This site is unofficial and independent of the FDA.