meddevicedb.com FDA Device Reference

microINR System

K201185 Class II Traditional
Decision Date
2020-12-18
Sponsor / Applicant
Iline Microsystems, S.L.

Technical Specification

510(k) Submission ID K201185
Product Code GJS
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7750
Decision Date 2020-12-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

microINR System received FDA 510(k) clearance under submission number K201185, sponsored by Iline Microsystems, S.L.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2020-12-18.

Classification & Regulation

This clearance is catalogued under FDA product code GJS and 21 CFR 864.7750, within the Hematology review panel as a Class II device.