Ortho Diagnostic Systems, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ortho Diagnostic Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: ORTHO-MUNE OKT 4A (CD4) - MONOCLONAL ANTIBODY (MURINE) FITC CONJUGATE, ORTHO-MUNE OK-COMBO CONTROL IGG2A-FITC/IGG2A-PE MONOCLONAL ANTIBODY (MURINE), ORTHO-MUNE OKB (CD19)- MONOCLONAL ANTIBODY (MURINE) PHYCOERYTHRINE CONJUGATE
Ortho Diagnostic Systems, Inc. has 126 FDA 510(k) cleared medical devices. Based in Carpinteria, US.
Historical record: 126 cleared submissions from 1981 to 1997. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Ortho Diagnostic Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ortho Diagnostic Systems, Inc.
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