Clearance Summary
IG_PLEX CELIAC DGP PANEL received FDA 510(k) clearance under submission number K140691, sponsored by Sqi Diagnostics Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2014-11-06.
- Submission: K140691
- Applicant / Sponsor: Sqi Diagnostics Systems, Inc.
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class II
- Regulation citation: 21 CFR 866.5660
- Decision date: 2014-11-06
Classification & Regulation
This clearance is catalogued under FDA product code MVM and 21 CFR 866.5660, within the Immunology review panel as a Class II device.