meddevicedb.com FDA Device Reference

BD Phoenix™ Automated Microbiology System

K250344 Class II Special
Decision Date
2025-03-06
Sponsor / Applicant
Becton, Dickinson and Company

Technical Specification

510(k) Submission ID K250344
Product Code LON
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.1645
Decision Date 2025-03-06
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BD Phoenix™ Automated Microbiology System received FDA 510(k) clearance under submission number K250344, sponsored by Becton, Dickinson and Company. The device was reviewed via the Special premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2025-03-06.

Classification & Regulation

This clearance is catalogued under FDA product code LON and 21 CFR 866.1645, within the Microbiology review panel as a Class II device.