meddevicedb.com FDA Device Reference

LabPro Data Management System

K201405 Class II Traditional
Decision Date
2020-08-30
Sponsor / Applicant
Beckman Coulter, Inc.

Technical Specification

510(k) Submission ID K201405
Product Code LON
Medical Specialty / Panel Microbiology
Regulation Citation 21 CFR 866.1645
Decision Date 2020-08-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LabPro Data Management System received FDA 510(k) clearance under submission number K201405, sponsored by Beckman Coulter, 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 2020-08-30.

Classification & Regulation

This clearance is catalogued under FDA product code LON and 21 CFR 866.1645, within the Microbiology review panel as a Class II device.