Device |
kit, rna detection, human papillomavirus |
Definition |
For the detection of human papillomavirus RNA to aid in assessing risk of cancer. |
Physical State |
Device is supplied as an in vitro diagnositc kit containing various reagents, instructions for use and possibly instrumentation and software. |
Technical Method |
Utilizes nucleic acid probes and/or primers along with other reagents to detect human papillomavirus RNA directly from human specimens |
Target Area |
Currently, this type of device is only utilized on cervical specimens, but other specimen types are possible. |
Review Panel |
Microbiology |
Product Code | OYB |
Premarket Review |
Office of In Vitro Diagnostics
(OHT7)
Division of Microbiology Devices
(DMD)
|
Submission Type |
PMA
|
Device Class |
3
|
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 |