meddevicedb.com FDA Device Reference

BACT/ALERT MP CULTURE BOTTLES (PLASTIC)

K031737 Class I Traditional
Decision Date
2003-07-14
Sponsor / Applicant
bioMerieux, Inc.

Technical Specification

510(k) Submission ID K031737
Product Code MDB
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.2560
Decision Date 2003-07-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BACT/ALERT MP CULTURE BOTTLES (PLASTIC) received FDA 510(k) clearance under submission number K031737, sponsored by bioMerieux, 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 2003-07-14.

Classification & Regulation

This clearance is catalogued under FDA product code MDB and 21 CFR 866.2560, within the Microbiology review panel as a Class I device.