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Tridak Division of Indicon, Inc.

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K891007	NONIMPLANTED ELECTRICAL CONTINENCE DEVICE	KPI	1990-06-07	View
510(k)	K860744	OPTHALMIC SURGICAL INSTRUMENTS	HMX	1986-03-31	View
510(k)	K853059	LABORIE FIBEROPTIC PRESSURE SENSOR & INTERFACE	FAP	1986-01-10	View
510(k)	K852856	LABORIE URODYNAMICS PROCESSOR	FAP	1985-10-17	View
510(k)	K851934	CYTOLOGICAL CERVICAL SPATULA THE MULTI-SPATULA	HHT	1985-07-05	View
510(k)	K842609	R.L. MEDICAL TWIN LIGHT SOURCE	FCW	1984-08-09	View
510(k)	K840605	LABORIE FIBREOPTIC LIGHT CABLE	FFS	1984-04-13	View

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