Medical Device Manufacturer · US , Mchenry , IL

Dade, Baxter Travenol Diagnostics, Inc. - FDA 510(k) Cleared Devices

44 submissions · 44 cleared · Since 1976

Total

Cleared

Denied

Dade, Baxter Travenol Diagnostics, Inc. has 44 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 44 cleared submissions from 1976 to 1980. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by Dade, Baxter Travenol Diagnostics, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Dade, Baxter Travenol Diagnostics, Inc.

44 devices

1-12 of 44

Cleared Mar 05, 1980

WHOLE BLOOD GAS CONTROL, LEVELS 1,2,&3

K800296 · GGM

Chemistry · 23d

Cleared Feb 13, 1980

WHOLE BLOOD PLATELET CONTROL NORMAL,

T3 UPTAKE (T3U) REAGENTS

FERRITIN RADIOIMMUNOASSAY

K792442 · DBF

Immunology · 19d

Cleared Nov 27, 1979

HARLECO BRAND CLINICARD LIPASE TEST SET

K791922 · CET

Chemistry · 62d

Cleared Nov 13, 1979

DADE HIGH DENSITY LIPOPROTEIN CHOLESTERO

K792183 · LBS

Chemistry · 15d

Cleared May 23, 1979

IMMU-TEK AUTOMATIC CENTRIFUGE

K790767 · KSN

Hematology · 34d

Cleared May 23, 1979

DADE LOW IONIC STRENGTH SOLUITION (LISS)

DATA-TOPE TRI-RAC RADIOASSAY CONTROL

K790264 · JJY

Chemistry · 43d

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Dade, Baxter Travenol Diagnostics, Inc. - FDA 510(k) Cleared Devices

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