meddevicedb.com FDA Device Reference

INFINITI SYSTEM

K060564 Class II Traditional
Decision Date
2007-02-07
Sponsor / Applicant
AutoGenomics, Inc.

Technical Specification

510(k) Submission ID K060564
Product Code NPQ
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7280
Decision Date 2007-02-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INFINITI SYSTEM received FDA 510(k) clearance under submission number K060564, sponsored by AutoGenomics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2007-02-07.

Classification & Regulation

This clearance is catalogued under FDA product code NPQ and 21 CFR 864.7280, within the Hematology review panel as a Class II device.