Medical Device Manufacturer · US , Mchenry , IL

Dako Corp. - FDA 510(k) Cleared Devices

54 submissions · 54 cleared · Since 1981

54

Total

54

Cleared

0

Denied

FDA 510(k) Regulatory Record - Dako Corp. Pathology ✕

5 devices

1-5 of 5

Cleared Feb 28, 2002

DAKO MONOCLONAL MOUSE ANTI-HUMAN PROGESTERONE RECEPTOR, CLONE PGR 636,...

Pathology · 56d

Cleared Mar 03, 2000

DAKO MONOCLONAL MOUSE ANTI-HUMAN ESTROGEN RECEPTOR

Pathology · 102d

Cleared Jul 13, 1982

DAKO PAP KIT K509

Pathology · 155d

Cleared Feb 10, 1982

DAKO PAP KIT K505

Pathology · 163d

Cleared Feb 10, 1982

DAKO PAP KIT K504

Pathology · 163d