Ortho Diagnostic Systems, Inc.
Ortho Diagnostic Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 1997.
Clearances by Ortho Diagnostic Systems, Inc. — page 2
101–126 of 126- K823131 — KOAGULAB 40-A AUTOMATED COAGULATION SYS
- K822782 — ACUSCREEN
- K821949 — ORTHO* ALTERNATIVE PATHWAY COMPL. TEST
- K821975 — ORTHO*-BI-LEVEL ASSAYED WHOLE BLOOD TOX
- K821026 — BI-LEVEL ASSAYED TUMOR MARKER & ANTIN
- K821898 — ORTHO CLASSICAL PATHWAY COMPL. TEST
- K820643 — ORTHO SPECTRUM III & ORTHO-MUNE OK
- K821806 — ORTHO CLG IMMUNE COMPLEX TEST SYSTEM
- K820199 — FETALSCREEN
- K820400 — ORTHO* HEMATOLOGY CONTROL 8 NORMAL
- K820392 — ORTHO* BI-LEVEL ASSAYED ALCOHOL DILUEN
- K820255 — BI-LEVEL ASSAYED URINE METAL CONTROL
- K813293 — ORTHO CO2 DILUENT LEVEL I
- K813294 — ORTHO CO2 DILUENT LEVEL II
- K813295 — ORTHO CO2 DILUENT LEVEL III
- K813321 — ORTHO* UNASSAYED CONTROL SERUM LEVEL I
- K813322 — ORTHO* UNASSAYED CONTROL SERUM LEVEL III
- K813167 — ORTHO UNASSAYED CONTROL SERUM LEVEL II
- K812002 — ELUAID
- K811713 — AVI-D CONTROL
- K811567 — ORTHO* BI-LEVEL ASSAYED GLYCOH. CONTR. S
- K811894 — ORTHO SICKLE CELL CONTROLS
- K811465 — IMIPRAMINE/DISIPRAMINE/LITHIUM
- K811466 — AMITRIPTYLINE/NORTRIPTYLINE/LITHIUM
- K811467 — DOXEPIN/DESMETHLDOXEPIN/LITHIUM
- K810058 — ORTHO QUANTITATIVE FIBRINOGEN ASSAY
Data sourced from openFDA. This site is unofficial and independent of the FDA.