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Tpl-Cordis, Inc.

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K885240	MODIFIED ANCOR & HI-FLEX UNIPOLAR ACTIVE FIX. LEAD	DTB	1989-02-10	View
510(k)	K882429	MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004	KRG	1988-07-22	View
510(k)	K880898	MULTICOR AND PACEMAKERS	DXY	1988-05-06	View
510(k)	K880432	VICOR PACER, MODEL 410A	DXY	1988-02-22	View
510(k)	K873158	MODIFIED MULTICOR AND OMNI-STANICOR PACEMAKERS	DXY	1988-01-07	View
510(k)	K873202	VICOR, MODEL 410A	DXY	1987-10-15	View

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