meddevicedb.com FDA Device Reference

BioFire Warrior Panel; BioFire Warrior Panel Control Kit

K243822 Traditional
Decision Date
2025-03-12
Sponsor / Applicant
Biofire Defense, LLC

Technical Specification

510(k) Submission ID K243822
Product Code PRD
Medical Specialty / Panel Immunology
Decision Date 2025-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BioFire Warrior Panel; BioFire Warrior Panel Control Kit received FDA 510(k) clearance under submission number K243822, sponsored by Biofire Defense, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2025-03-12.

Classification & Regulation

This clearance is catalogued under FDA product code PRD , within the Immunology review panel as a device.