MAQ — Kit, Dna Detection, Human Papillomavirus Class III

FDA Device Classification

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

Classification Details

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