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VERIGENE ENTERIC PATHOGEN NUCLEIC ACID TEST (EP)

K142033 Class II Traditional
Decision Date
2014-10-10
Sponsor / Applicant
Nanospere,Inc.

Technical Specification

510(k) Submission ID K142033
Product Code PCH
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3990
Decision Date 2014-10-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VERIGENE ENTERIC PATHOGEN NUCLEIC ACID TEST (EP) received FDA 510(k) clearance under submission number K142033, sponsored by Nanospere,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 2014-10-10.

Classification & Regulation

This clearance is catalogued under FDA product code PCH and 21 CFR 866.3990, within the Microbiology review panel as a Class II device.