QYV

Digital Cervical Cytology Slide Imaging System With Artificial Intelligence Algorithm

Product code
QYV
Device name
Digital Cervical Cytology Slide Imaging System With Artificial Intelligence Algorithm
Device class
Class 2
21 CFR
21 CFR 864.3900
Medical specialty
Pathology
Marketing pathway
510(K)
510(k) clearances (last 3 years)
1
Summaries archived here
0 (direct download)
510(k) clearances (all years, FDA)
1 (all years; only the last 3 years are listed here)

FDA classification definition

The digital cervical cytology slide imaging system with artificial intelligence (AI) algorithm is a prescription in vitro diagnostic device consisting of an automated digital slide creation, viewing, and management system intended to aid in the review of digital images of slides prepared from Pap test specimens and conventional Pap smears by selecting and presenting areas of interest to facilitate interpretation by the reader. The AI software algorithm uses machine learning techniques to provide information to the user about the presence, location, or characteristics of areas of the image with clinical implications. Information from this device is intended to assist the user in rendering a cytology diagnosis.

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

510(k) clearances, last 3 years (1)

Last three years. Most recent: 2024-01-31.

NumberDecision dateApplicantDevice nameSummary
DEN2100352024-01-31Hologic, Inc.“Genius™ Digital Diagnostics System with the Genius™…
Official FDA classification page: QYV
Classification and pathway per current FDA publications. Data from openFDA (CC0).