Ortho Diagnostics, Inc.
FDA 510(k) medical device clearances.
Top product codes for Ortho Diagnostics, Inc.
Recent clearances by Ortho Diagnostics, Inc.
- K802404 — ORTHO BOVINE ALBUMIN SOLUTION 30% PROTE
- K801507 — ANTIGEN CONTROL CELLS
- K800357 — BI-LEVEL ASSAYED CARD. DRUG CONT., I,II
- K800310 — ORTHO ANTISERA CONTROL
- K791791 — ORTHO ANTIBODY ENHANCEMENT SOLUTION
- K791301 — ORTHO TSH RIA KIT
- K790813 — MULTECON BLOOD GAS CONTROL
- K782063 — PREGNANCY, SENSIDEX TUBE TEST
- K782166 — SLIDE TEST FOR PREGNANCY, GRAVINDEX 90
- K781638 — RUBINDEX*DIRECT SYSTEM
- K781860 — ASSAY, CHROMOGENIC ANTITHROMBIN III
- K781572 — NORMAL HEMATOLOGY CONTROL UNASSAYED
- K781573 — ABNORMAL HEMATOLOGY CONTROL UNASSAYED
- K781481 — ORTHO*T-3 RIA (PEG) KIT
- K781482 — ORTHO*T-3 UPTAKE KIT
- K781483 — ORTHO*T-4 RIA (PEG) KIT
- K781435 — ORTHO LOW IONIC SOLUTION
- K781335 — DIGOXIN RIA (PEG) KIT
- K781104 — PLASMA COAGULATION CONT., ABNORMAL
- K780002 — ANTITHROMBIN III ASSAY
- K771487 — LEWIS BLOOD GROUP SUBSTANCE
- K771488 — P1 BLOOD GROUP SUBSTANCE
- K771814 — REAGENT CONFIDENCE SERA
- K761137 — MICROSAMPLE BLOOD COLLECTION DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.