meddevicedb.com FDA Device Reference

BD Enteric Bacterial Panel for BD COR System, BD Enteric Bacterial Panel plus for BD COR System, and Enteric Bacterial Panel Diluent for BD COR System

K250358 Class II Traditional
Decision Date
2025-10-31
Sponsor / Applicant
Becton, Dickinson and Company

Technical Specification

510(k) Submission ID K250358
Product Code PCI
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3990
Decision Date 2025-10-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BD Enteric Bacterial Panel for BD COR System, BD Enteric Bacterial Panel plus for BD COR System, and Enteric Bacterial Panel Diluent for BD COR System received FDA 510(k) clearance under submission number K250358, sponsored by Becton, Dickinson and Company. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 2025-10-31.

Classification & Regulation

This clearance is catalogued under FDA product code PCI and 21 CFR 866.3990, within the Microbiology review panel as a Class II device.