meddevicedb.com FDA Device Reference

CAPI 3 Immunotyping, Capillarys 3 Tera

K192095 Class II Traditional
Decision Date
2019-11-01
Sponsor / Applicant
Sebia

Technical Specification

510(k) Submission ID K192095
Product Code CFF
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5510
Decision Date 2019-11-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CAPI 3 Immunotyping, Capillarys 3 Tera received FDA 510(k) clearance under submission number K192095, 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 2019-11-01.

Classification & Regulation

This clearance is catalogued under FDA product code CFF and 21 CFR 866.5510, within the Immunology review panel as a Class II device.