meddevicedb.com FDA Device Reference

IDS SS-A/Ro; IDS SS-A/Ro 60 kDa; IDS SS-B/La

K253817 Class II Traditional
Decision Date
2026-08-21
Sponsor / Applicant
Immunodiagnostics Systems Limited

Technical Specification

510(k) Submission ID K253817
Product Code LLL
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5100
Decision Date 2026-08-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IDS SS-A/Ro; IDS SS-A/Ro 60 kDa; IDS SS-B/La received FDA 510(k) clearance under submission number K253817, sponsored by Immunodiagnostics Systems Limited. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2026-08-21.

Classification & Regulation

This clearance is catalogued under FDA product code LLL and 21 CFR 866.5100, within the Immunology review panel as a Class II device.