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iC-GN iC-Cassette for use on the iC-System

K190341 Class II Traditional
Decision Date
2019-06-28
Sponsor / Applicant
Icubate, Inc.

Technical Specification

510(k) Submission ID K190341
Product Code PEN
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.3365
Decision Date 2019-06-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

iC-GN iC-Cassette for use on the iC-System received FDA 510(k) clearance under submission number K190341, sponsored by Icubate, 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 2019-06-28.

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.