FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

ORTHO BI-LEVEL RECEPTOR CONTROL

K Number: K834064 · Decision Mar 23, 1984
Classifications
1
FEI Numbers
127
Registration Numbers
127
Same Product Code
672
Applicant Total
126
Review Days
119

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Basic Information

Device Name
ORTHO BI-LEVEL RECEPTOR CONTROL
K Number
K834064
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Ortho Diagnostic Systems, Inc.
Date Received
November 25, 1983
Decision Date
March 23, 1984
Product Code
JJY
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JJY Multi-Analyte Controls, All Kinds (Assayed)

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Other Clearances by Ortho Diagnostic Systems, Inc.

K Number Device Name
K951459 ORTHO-MUNE OKT 4A (CD4) - MONOCLONAL ANTIBODY (MURINE) FITC CONJUGATE
K951632 ORTHO-MUNE OK-COMBO CONTROL IGG2A-FITC/IGG2A-PE MONOCLONAL ANTIBODY (MURINE)
K964754 ORTHO-MUNE OKB (CD19)- MONOCLONAL ANTIBODY (MURINE) PHYCOERYTHRINE CONJUGATE
K963902 QUANTITATIVE FIBRINOGEN ASSAY
K950625 ORTHO-MUNE OK-COMBO CD40FITC/CD8-PE (OKT4A/OKT8) MONOCLONAL ANTIBODY (MURINE)
K951100 ORTHO-MUNE OK-COMBO CD3-FITC/CD19-PE (OKT3/OKB19A MONOLCLONAL ANTIBODY (MURINE)
K950568 ORTHO-MUNE OK-COMBO CD3-FITC/CD4-PE (OKT2/OKT4A) MONOCLONAL ANTIBODY (MURINE)
K950482 ORTHO-MUNE OK-COMVO CD3-FITC/CD8-PE (OKT 3/OKT8) MONOCLONAL ANTIBODY (MURINE)
K935720 ORTHO COUNT CALIBRATION KIT FOR ORTHO CYTORONABSOLUTE LASER FLOW CYTOMETRY SYSTEM
K954570 ORTHO IMMUNOCOUNT FLOW CYTOMETRY SYSTEM
Search all 126 clearances from Ortho Diagnostic Systems, Inc. →