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U.S. Department of Health and Human Services

Product Classification

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Device kappa and lambda immunoglobulin light chain in situ hybridization mrna probe detection kit
Definition A kappa and lambda immunoglobulin light chain in situ hybridization (ISH) mRNA probe is intended as an aid in the identification of hematolymphoid neoplasms using in situ hybridization. A Kappa and Lambda ISH mRNA probe cocktail is indicated for use when a hematolymphoid biopsy (e.g., bone marrow, lymphoid tissue) yields inconclusive results. The assay is intended as an aid in the diagnosis of mature B-cell lymphomas and plasma cell neoplasms
Physical State May include chromogenically or fluorescently labeled oligonucleotide mRNA probes targeting kappa and lambda light chain mRNA and required ancillary reagents.
Technical Method Hematolymphoid cells of interest are hybridized with nucleic acid probes for determining kappa and lambda mRNA ratios using ISH a clinically validated algorithm to determine the immunoglobulin light chain restriction status. Hybridization may be performed manually or using an automated stainer.
Target Area Human clinical hematolymphoid specimens, including formalin-fixed, paraffin-embedded bone marrow aspirates and lymphoid tissue specimens.
Regulation Medical Specialty Hematology
Review Panel Molecular Genetics
Product CodeSDP
Premarket Review Division of Molecular Genetics and Pathology (DMGP)
Division of Molecular Genetics and Pathology (DMGP)
Submission Type 510(k)
Regulation Number 864.1861
Device Class 2
Total Product Life Cycle (TPLC) TPLC Product Code Report
GMP Exempt? No
Summary Malfunction
Reporting
Ineligible
Implanted Device? No
Life-Sustain/Support Device? No
Third Party Review Not Third Party Eligible
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