OYB — Kit, Rna Detection, Human Papillomavirus Class III

FDA Device Classification

FDA product code OYB covers "Kit, Rna Detection, Human Papillomavirus", a Class III medical device. Submissions are reviewed by the Unknown panel.

Classification Details

Product Code
OYB
Device Class
Class III
Regulation Number
Submission Type
Review Panel
MI
Medical Specialty
Unknown
Implant
No

Definition

For the detection of human papillomavirus RNA to aid in assessing risk of cancer.