meddevicedb.com FDA Device Reference

INTEGRATED LABORATORY AUTOMATION SOLUTION

K091975 Class II Traditional
Decision Date
2010-03-10
Sponsor / Applicant
Integrated Laboratory Automation Solutions, Inc.

Technical Specification

510(k) Submission ID K091975
Product Code CGA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2010-03-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INTEGRATED LABORATORY AUTOMATION SOLUTION received FDA 510(k) clearance under submission number K091975, sponsored by Integrated Laboratory Automation Solutions, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2010-03-10.

Classification & Regulation

This clearance is catalogued under FDA product code CGA and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.