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BACT/ALERT 3D MICROBIAL DETECTION SYSTEM

K981736 Class I Traditional
Decision Date
1998-07-24
Sponsor / Applicant
Organon Teknika Corp.

Technical Specification

510(k) Submission ID K981736
Product Code MDB
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.2560
Decision Date 1998-07-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BACT/ALERT 3D MICROBIAL DETECTION SYSTEM received FDA 510(k) clearance under submission number K981736, 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 1998-07-24.

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.