Medical Device Manufacturer · US , Mchenry , IL

Davis & Geck, Inc. - FDA 510(k) Cleared Devices

45 submissions · 42 cleared · Since 1981

45

Total

42

Cleared

0

Denied

FDA 510(k) Regulatory Record - Davis & Geck, Inc. Cardiovascular ✕

4 devices

1-4 of 4

Cleared Mar 15, 1996

FLEXON TEMPORARY CARDIAC PACER LEAD

Cardiovascular · 88d

Cleared Aug 21, 1995

TETRAFLUOROETHYLENE (TFE) POLYMER PLEDGET

Cardiovascular · 38d

Cleared Aug 21, 1995

POLYETHYLENE TEREPHTHALATE (PET) PLEDGET

Cardiovascular · 31d

Cleared Feb 26, 1986

FLEXON TEMPORARY CARDIAC CONDUCTIVE MULTIFILAMENT

Cardiovascular · 65d