Dade, Baxter Travenol Diagnostics, Inc.
FDA 510(k) medical device clearances.
Top product codes for Dade, Baxter Travenol Diagnostics, Inc.
Recent clearances by Dade, Baxter Travenol Diagnostics, Inc.
- K800296 — WHOLE BLOOD GAS CONTROL, LEVELS 1,2,&3
- K792606 — WHOLE BLOOD PLATELET CONTROL NORMAL,
- K792723 — BLOOD FLUID FILTERS
- K792607 — T3 UPTAKE (T3U) REAGENTS
- K792443 — TSH RADIOIMMUNOASSAY
- K792442 — FERRITIN RADIOIMMUNOASSAY
- K791922 — HARLECO BRAND CLINICARD LIPASE TEST SET
- K792183 — DADE HIGH DENSITY LIPOPROTEIN CHOLESTERO
- K790767 — IMMU-TEK AUTOMATIC CENTRIFUGE
- K790776 — DADE LOW IONIC STRENGTH SOLUITION (LISS)
- K790571 — QUIK-STAIN
- K790264 — DATA-TOPE TRI-RAC RADIOASSAY CONTROL
- K790204 — PLASMA, STANDARDIZED NORMAL
- K781479 — HEPARIN ASSAY
- K782150 — FLUROMETER, DADE
- K782098 — REAGENT, LYSING AND HEMOGLOBIN
- K781478 — PLASMINOGEN ASSAY
- K781480 — ANTITHROMBIN III ASSAY
- K781593 — RIA CONTROLS
- K781077 — CONTROL, HEMATOLOGY, CH-60
- K780801 — ISOZYME - ID CPK MARKER
- K780208 — ASPIRATOR, MANUEL
- K780047 — PLATELET AGGREGATING REAGENTS
- K780281 — IMMUFUGE DISP. LINER
- K771740 — CARDIOZYME CK-CONTROL LEVEL 1
- K770974 — CARDIOZYME CK-MB REAGENTS
- K771588 — PLATELET CONTROLS NORMAL & ABNORMAL
- K771346 — CI-TROL COAGULATION CONTROLS II & III
- K770971 — CARDIOZYME CK-CONTROL ABNORMAL
- K770973 — CARDIOZYME CK CONTROL NORMAL
- K771137 — PIPETS UNIFORM DROP SIZE BOROSILICATE
- K771138 — PIPETS BOROSILICATE GLASS
- K770950 — WHOLE BLOOD GAS CONTROL
- K770972 — CARDIOZYME CK-TOTAL REAGENTS
- K761283 — TRI-CON TRIGLYCERIDGE REAGENTS
- K761281 — DATA-TOPE T3 UPTAKE PROCEDURE
- K761284 — UNIVAL CONTROL CELLS
- K761282 — DATA-TOPE T4 RIA PROCEDURE
- K761303 — IMMU-SAL IMMUNOHEMATOLOGICAL SALINE
- K760594 — AUTO-FI COAGULATION INSTRUMENT
- K760719 — UNIFORM DROP SIZE PASTEUR TYPE PIPETS
- K760549 — PLATELET CONTROLS, NORMAL & ABNORMAL
- K760416 — DATA-TOPE SYSTEM DIGOXIN RIA
- K760318 — ACTIN, ACTIVATED CEPHALOPLASTIN REAGENT
Data sourced from openFDA. This site is unofficial and independent of the FDA.