FDA Product Code QDC: Dna-based Test For Minimal Residual Disease For Hematologic Malignancies
A Dna-based Test For Minimal Residual Disease Is An In Vitro Diagnostic Device That Identifies And Quantifies Specific Nucleic Acid Sequences Isolated From Human Specimens To Estimate The Percentage Of Cells That Harbor The Specific Sequence(s). The Test Is Intended To Be Used As An Aid To Measure Minimal Residual Disease To Monitor The Change In Burden Of Disease For Patients With A Hematological Malignancy During And After Treatment. The Results Should Be Interpreted By A Pathologist Or Equivalent Professional In Conjunction With Other Clinical And Laboratory Findings.
Leading manufacturers include Adaptive Biotechnologies Corporation.
2
Total
1
Cleared
290d
Avg days
2018
Since
FDA 510(k) Cleared Dna-based Test For Minimal Residual Disease For Hematologic Malignancies Devices (Product Code QDC)
2 devices
Cleared
Aug 05, 2020
Adaptive Biotechnologies clonoSEQ Assay
Adaptive Biotechnologies Corporation
Medical Genetics
216d
Not Cleared
Sep 28, 2018
Adaptive Biotechnologies clonoSEQ Assay
Adaptive Biotechnologies Corporation
Pathology
364d