Medical Device Manufacturer · US , Mchenry , IL

Anatech, Ltd. - FDA 510(k) Cleared Devices

14 submissions · 14 cleared · Since 1984

Total

Cleared

Denied

Anatech, Ltd. has 14 FDA 510(k) cleared pathology devices. Based in Mchenry, US.

Historical record: 14 cleared submissions from 1984 to 1988.

Browse the complete list of FDA 510(k) cleared pathology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Anatech, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Anatech, Ltd.

14 devices

1-14 of 14

ZINC FORMALIN CONCENTRATE

ANATECH HEMATOXYLIN-NORMAL STRENGTH

K872499 · HYJ

Pathology · 15d

Cleared Jul 09, 1987

ANATECH HEMATOXYLIN-EXTRA STRENGTH

K872500 · HYJ

Pathology · 15d

Cleared Mar 31, 1987

NBF 10% NEUTRAL BUFFERED FORMALIN

REFRAX MOUNTING MEDIUM

K842986 · LEB

Pathology · 22d

Anatech, Ltd. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Anatech, Ltd.

Filters