MKQ
- Product code
- MKQ
- Device name
- Processor, Cervical Cytology Slide, Automated
- Device class
- Class 3
- Medical specialty
- Unknown
- Marketing pathway
- PMA
FDA classification definition
It is a system that is used to collect and prepare cervical cytology specimens for Pap stain-based screening for cervical cancer. The specimens are collected and rinsed into a liquid preservative fluid from which they are then automatically filtered and deposited in a thin-layer on a glass microscope slide. They are stained and screened by a cytotechnologist and cytopathologist.
Official FDA classification page: MKQ
Classification and pathway per current FDA publications. Data from openFDA (CC0).