meddevicedb.com FDA Device Reference

Panther Fusion SARS-CoV-2/Flu A/B/RSV Assay

K222736 Class II Traditional
Decision Date
2023-05-16
Sponsor / Applicant
Hologic, Inc.

Technical Specification

510(k) Submission ID K222736
Product Code QOF
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3981
Decision Date 2023-05-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Panther Fusion SARS-CoV-2/Flu A/B/RSV Assay received FDA 510(k) clearance under submission number K222736, sponsored by Hologic, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2023-05-16.

Classification & Regulation

This clearance is catalogued under FDA product code QOF and 21 CFR 866.3981, within the Microbiology review panel as a Class II device.