Tpl-Cordis, Inc.

6 FDA 510(k) medical device clearances.

Top product codes for Tpl-Cordis, Inc.

Recent clearances by Tpl-Cordis, Inc.

K885240 — MODIFIED ANCOR & HI-FLEX UNIPOLAR ACTIVE FIX. LEAD DTB · 1989-02-10
K882429 — MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004 KRG · 1988-07-22
K880898 — MULTICOR AND PACEMAKERS DXY · 1988-05-06
K880432 — VICOR PACER, MODEL 410A DXY · 1988-02-22
K873158 — MODIFIED MULTICOR AND OMNI-STANICOR PACEMAKERS DXY · 1988-01-07
K873202 — VICOR, MODEL 410A DXY · 1987-10-15

Data sourced from openFDA. This site is unofficial and independent of the FDA.