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VERIGENE GRAM NEGATIVE BLOOD CULTURE NUCLEIC ACID TEST (BC-GN)

K132843 Class II Traditional
Decision Date
2014-01-08
Sponsor / Applicant
Nanosphere, Inc.

Technical Specification

510(k) Submission ID K132843
Product Code PEN
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3365
Decision Date 2014-01-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VERIGENE GRAM NEGATIVE BLOOD CULTURE NUCLEIC ACID TEST (BC-GN) received FDA 510(k) clearance under submission number K132843, sponsored by Nanosphere, 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 2014-01-08.

Classification & Regulation

This clearance is catalogued under FDA product code PEN and 21 CFR 866.3365, within the Microbiology review panel as a Class II device.