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BACT/ALERT FA PLUS CULTURE BOTTLE

K121461 Class I Traditional
Decision Date
2013-01-22
Sponsor / Applicant
bioMerieux, Inc.

Technical Specification

510(k) Submission ID K121461
Product Code MDB
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.2560
Decision Date 2013-01-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BACT/ALERT FA PLUS CULTURE BOTTLE received FDA 510(k) clearance under submission number K121461, 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 2013-01-22.

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.