Last synced on 30 May 2025 at 11:05 pm

Jak2 Gene Mutation Detection Test

Page Type
Product Code
Definition
The JAK2 gene mutation detection system is a device used to detect mutations and variants in the JAK2 gene. It is intended for use as an adjunct to evaluation of suspected Polycythemia Vera, in conjunction with other clinicopathological factors.
Physical State
The test utilizes a multiplex qualitative amplification based detection system. It may also utilize other technologies and/or quantification methods.
Technical Method
The test is a quantitative real time PCR that uses specific primers and probes for selective amplification of mutant and wild type alleles for detection of gene mutations.
Target Area
Human peripheral whole blood.
Regulation Medical Specialty
Medical Genetics
Review Panel
Pathology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.6070
GMP Exempt?
No
Summary Malfunction Reporting
Eligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code PSU is linked to regulation 21CFR866.6070, which does not seem to exist yet. It may be pending at the moment.

Jak2 Gene Mutation Detection Test

Page Type
Product Code
Definition
The JAK2 gene mutation detection system is a device used to detect mutations and variants in the JAK2 gene. It is intended for use as an adjunct to evaluation of suspected Polycythemia Vera, in conjunction with other clinicopathological factors.
Physical State
The test utilizes a multiplex qualitative amplification based detection system. It may also utilize other technologies and/or quantification methods.
Technical Method
The test is a quantitative real time PCR that uses specific primers and probes for selective amplification of mutant and wild type alleles for detection of gene mutations.
Target Area
Human peripheral whole blood.
Regulation Medical Specialty
Medical Genetics
Review Panel
Pathology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
866.6070
GMP Exempt?
No
Summary Malfunction Reporting
Eligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code PSU is linked to regulation 21CFR866.6070, which does not seem to exist yet. It may be pending at the moment.