Clearance Summary
FIAX IGG TEST received FDA 510(k) clearance under submission number K832821, sponsored by Intl. Diagnostic Technology. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1983-10-14.
- Submission: K832821
- Applicant / Sponsor: Intl. Diagnostic Technology
- Clearance pathway: Traditional
- Review panel: Immunology
- Device class: Class I
- Regulation citation: 21 CFR 866.5860
- Decision date: 1983-10-14
Classification & Regulation
This clearance is catalogued under FDA product code DFI and 21 CFR 866.5860, within the Immunology review panel as a Class I device.