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 Code | SDP |
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 |