Medical Device Manufacturer · US , Suffield , CT

Tpl-Cordis, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1987

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Tpl-Cordis, Inc. Cardiovascular ✕

6 devices

1-6 of 6

Cleared Feb 10, 1989

MODIFIED ANCOR & HI-FLEX UNIPOLAR ACTIVE FIX. LEAD

Cardiovascular · 51d

Cleared Jul 22, 1988

MODEL 255A PROGRAMMER III, W/SOFTWARE REVI. 4004

Cardiovascular · 38d

Cleared May 06, 1988

MULTICOR AND PACEMAKERS

Cardiovascular · 70d

Cleared Feb 22, 1988

VICOR PACER, MODEL 410A

Cardiovascular · 25d

Cleared Jan 07, 1988

MODIFIED MULTICOR AND OMNI-STANICOR PACEMAKERS

Cardiovascular · 150d

Cleared Oct 15, 1987

VICOR, MODEL 410A

Cardiovascular · 63d