Device |
group a streptococcus nucleic acid amplification assay system |
Definition |
An in vitro diagnostic test for the detection of Streptococcuc pyogenes (Group A beta hemolytic Streptococcus) in throat swab specimens from symptomatic patients. |
Physical State |
May include automated/manual isothermal nucleic acid amplification, polymerase chain reaction, ligase chain reaction, sequence-based amplification |
Technical Method |
Uses nucleic acid amplification technology to detect Group A Sreptococci |
Target Area |
Throat Swab Specimen |
Regulation Medical Specialty |
Microbiology |
Review Panel |
Microbiology |
Product Code | OYZ |
Premarket Review |
Division of Microbiology Devices
(DMD)
Division of Microbiology Devices
(DMD)
|
Submission Type |
510(k)
|
Regulation Number |
866.3740
|
Device Class |
1
|
Total Product Life Cycle (TPLC) |
TPLC Product Code Report
|
GMP Exempt? |
No
|
Summary Malfunction Reporting |
Eligible |
Implanted Device? |
No
|
Life-Sustain/Support Device? |
No
|
Third Party Review |
Not Third Party Eligible |