meddevicedb.com FDA Device Reference

FLC Kappa, FLC Lambda, FLC Control Level 1, FLC Control Level 2

K210623 Class II Traditional
Decision Date
2022-11-18
Sponsor / Applicant
Sebia

Technical Specification

510(k) Submission ID K210623
Product Code DFH
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5550
Decision Date 2022-11-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLC Kappa, FLC Lambda, FLC Control Level 1, FLC Control Level 2 received FDA 510(k) clearance under submission number K210623, sponsored by Sebia. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2022-11-18.

Classification & Regulation

This clearance is catalogued under FDA product code DFH and 21 CFR 866.5550, within the Immunology review panel as a Class II device.