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CAPI 3 IMMUNOTYPING, CAPILLARYS 3 TERA, IT/IF CONTROL

K161928 Class II Traditional
Decision Date
2016-12-21
Sponsor / Applicant
Sebia

Technical Specification

510(k) Submission ID K161928
Product Code CFF
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5510
Decision Date 2016-12-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CAPI 3 IMMUNOTYPING, CAPILLARYS 3 TERA, IT/IF CONTROL received FDA 510(k) clearance under submission number K161928, 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 2016-12-21.

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.