Ortho Diagnostics, Inc.
Ortho Diagnostics, Inc. holds FDA 510(k) medical device clearances, first cleared 1977, most recent 1980.
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.