Medical Device Manufacturer · US , Mchenry , IL

Diatech, Inc. - FDA 510(k) Cleared Devices

17 submissions · 17 cleared · Since 1984

Total

Cleared

Denied

Diatech, Inc. has 17 FDA 510(k) cleared hematology devices. Based in Mchenry, US.

Historical record: 17 cleared submissions from 1984 to 1988.

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

Diatech, Inc. 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 - Diatech, Inc.

17 devices

1-12 of 17

COASCREENER/DIASCREENERBLOOD PLASMA TIMING INST.

K854938 · JPA

Hematology · 92d

Cleared Jan 06, 1986

DIATIMER-1 BLOOD PLASMA CLOT TIMING INSTRUMENT

K854089 · JPA

Hematology · 91d

Cleared Jan 06, 1986

DIATIMER-2 BLOOD PLASMA CLOT TIMING INSTRUMENT

HEPARIN COAGULATION CONTROL PLASMA 1-

K841462 · JPA

Hematology · 53d

Cleared Jun 01, 1984

OWREN'S VERONAL BUFFERR

K841523 · JPA

Hematology · 50d

Cleared May 02, 1984

COAGULATION CONTROL PLASMA LEVEL 1/2/3

K841461 · GGP

Hematology · 23d

Cleared May 01, 1984

DIA THROMBIN DIA PLASTIN

K840802 · GJS

Hematology · 68d

Cleared Apr 30, 1984

FACTOR DEFICIENT SUBSTRATE PLASMA II

K840927 · GGP

Hematology · 59d

Diatech, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Diatech, Inc.

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