MKQ

Processor, Cervical Cytology Slide, Automated

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.

Definition text from the FDA device classification database (U.S. federal government work, public domain).

Official FDA classification page: MKQ
Classification and pathway per current FDA publications. Data from openFDA (CC0).