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BACTALERT FA

K992400 Class I Traditional
Decision Date
1999-09-03
Sponsor / Applicant
Organon Teknika Corp.

Technical Specification

510(k) Submission ID K992400
Product Code MDB
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.2560
Decision Date 1999-09-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BACTALERT FA received FDA 510(k) clearance under submission number K992400, sponsored by Organon Teknika Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Microbiology review panel. The statutory decision date of record is 1999-09-03.

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.