Tpl-Cordis, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K885240MODIFIED ANCOR & HI-FLEX UNIPOLAR ACTIVE FIX. LEADFebruary 10, 1989
K882429MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004July 22, 1988
K880898MULTICOR AND PACEMAKERSMay 6, 1988
K880432VICOR PACER, MODEL 410AFebruary 22, 1988
K873158MODIFIED MULTICOR AND OMNI-STANICOR PACEMAKERSJanuary 7, 1988
K873202VICOR, MODEL 410AOctober 15, 1987